Canonical Allele Identifier: CA1618277958
Gene: OR5V1 HGNC NCBI
OR12D3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29374998G= , CM000668.2:g.29374998G= GRCh38
NC_000006.11:g.29342775G= , CM000668.1:g.29342775G= GRCh37
NC_000006.10:g.29450754G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377154.1:c.-82-18721C= (OR5V1) ENSP00000366359.1:n.-82-18721C=
ENST00000396806.3:c.290C= (OR12D3) MANE Select ENSP00000380023.3:p.Thr97=
NM_030959.2:c.290C= (OR12D3) NP_112221.1:p.Thr97=
XM_011514929.1:c.-82-18721C= (OR5V1) XP_011513231.1:n.-82-18721C=
XM_011514930.1:c.-82-18721C= (OR5V1) XP_011513232.1:n.-82-18721C=
XM_011514931.1:c.-82-18721C= (OR5V1) XP_011513233.1:n.-82-18721C=
XM_011514932.1:c.-82-18721C= (OR5V1) XP_011513234.1:n.-82-18721C=
XM_011514930.2:c.-82-18721C= (OR5V1) XP_011513232.1:n.-82-18721C=
XM_024446562.1:c.-82-18721C= (OR5V1) XP_024302330.1:n.-82-18721C=
NM_030959.3:c.290C= (OR12D3) MANE Select NP_112221.1:p.Thr97=