Canonical Allele Identifier: CA363015899

Gene: OR5V1 OR12D3

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377154.1:c.-82-18721C>A (OR5V1)	ENSP00000366359.1:n.-82-18721C>A
ENST00000396806.3:c.290C>A (OR12D3) MANE Select	ENSP00000380023.3:p.Thr97Asn
NM_030959.2:c.290C>A (OR12D3)	NP_112221.1:p.Thr97Asn
XM_011514929.1:c.-82-18721C>A (OR5V1)	XP_011513231.1:n.-82-18721C>A
XM_011514930.1:c.-82-18721C>A (OR5V1)	XP_011513232.1:n.-82-18721C>A
XM_011514931.1:c.-82-18721C>A (OR5V1)	XP_011513233.1:n.-82-18721C>A
XM_011514932.1:c.-82-18721C>A (OR5V1)	XP_011513234.1:n.-82-18721C>A
XM_011514930.2:c.-82-18721C>A (OR5V1)	XP_011513232.1:n.-82-18721C>A
XM_024446562.1:c.-82-18721C>A (OR5V1)	XP_024302330.1:n.-82-18721C>A
NM_030959.3:c.290C>A (OR12D3) MANE Select	NP_112221.1:p.Thr97Asn