Many thanks!
Any way to do this in a more automatic way. I have 70 transcripts to check
Working in a clinical lab, we have a list of RefSeq transcripts used to targeted our analysis. My colleagues who carry out the variant interpretation are using a variant interpretation tool that having a variant, ask them to select in which transcripts you are working on. This tools is updating the versions of the transcripts (e.g. we have in our targeted transcripts list this NM_002734.4, however that version is not available in the program and now its show us this NM_002734.5). The program doesn't not allow you to type the transcripts you are working and (not sure) this may affect subsequence analysis.
I have been asked
1 Different transcript versions have different coordinates. I mean, could it be possible to find transcripts with different version and these have exons in different locations for example?? I would say no but I am not sure
To check that, is there a easy to check this?
You can find revision history of GenBank accession numbers using a special URL. For the accession you mention above you can see that information by going to https://www.ncbi.nlm.nih.gov/nuccore/NM_002734?report=girevhist
From there you can select appropriate buttons to see the differences between any two accession revisions: https://www.ncbi.nlm.nih.gov/sviewer/girevhist-diff/girevhist-diff.cgi?tool=portal&db=nuccore&frst=1779521771_4_432481692_Jun%209,%202022%2002:44%20AM_5_1&scnd=443497962_47_133370799_Sep%2025,%202019%2001:48%20AM_4_1&history_fmt=gb
BTW these two versions are rather different
Accession Gi Update Date
NM_002734.5 1779521771 Jun 9, 2022 02:44 AM
NM_002734.4 443497962 Sep 25, 2019 01:48 AM
LOCUS NM_002734 4253 bp mRNA linear PRI 09-JUN-2022
LOCUS NM_002734 4325 bp mRNA linear PRI 25-SEP-2019
Many thanks!
Any way to do this in a more automatic way. I have 70 transcripts to check
Use EntrezDirect and compare results:
$ esearch -db nuccore -query NM_002734.5 | efetch -format ft | grep -w -e exon -e gene
1 4253 gene
gene PRKAR1A
1 119 exon
120 302 exon
303 473 exon
474 565 exon
566 627 exon
628 674 exon
675 833 exon
834 894 exon
895 1016 exon
1017 1098 exon
1099 4253 exon
$ esearch -db nuccore -query NM_002734.4 | efetch -format ft | grep -w -e exon -e gene
1 4325 gene
gene PRKAR1A
1 170 exon
171 353 exon
354 524 exon
525 616 exon
617 678 exon
679 725 exon
726 884 exon
885 945 exon
946 1067 exon
1068 1149 exon
1150 4304 exon
Many thanks for your answer. Do you know how can I take the genomic coordinates?
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