Canonical Allele Identifier: CA2627389051

Gene: OCA2

Linked Data

• gnomAD v4: 15-28099117-T-TCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28099118_28099119insAGC , CM000677.2:g.28099118_28099119insAGC	GRCh38
NC_000015.9:g.28344264_28344265insAGC , CM000677.1:g.28344264_28344265insAGC	GRCh37
NC_000015.8:g.26017859_26017860insAGC	NCBI36
NG_009846.1:g.5195_5196insCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.-22+106_-22+107insCTG MANE Select	ENSP00000346659.3:n.-22+106_-22+107insCTG
ENST00000353809.9:c.-22+106_-22+107insCTG	ENSP00000261276.8:n.-22+106_-22+107insCTG
ENST00000354638.7:c.-22+106_-22+107insCTG	ENSP00000346659.3:n.-22+106_-22+107insCTG
ENST00000431101.1:c.-29_-28insCTG	ENSP00000415431.1:n.-29_-28insCTG
ENST00000445578.5:c.-22+106_-22+107insCTG	ENSP00000414425.1:n.-22+106_-22+107insCTG
NM_000275.2:c.-22+106_-22+107insCTG	NP_000266.2:n.-22+106_-22+107insCTG
NM_001300984.1:c.-22+106_-22+107insCTG	NP_001287913.1:n.-22+106_-22+107insCTG
XM_011521640.1:c.-22+106_-22+107insCTG	XP_011519942.1:n.-22+106_-22+107insCTG
XM_011521640.2:c.-22+106_-22+107insCTG	XP_011519942.1:n.-22+106_-22+107insCTG
NM_000275.3:c.-22+106_-22+107insCTG MANE Select	NP_000266.2:n.-22+106_-22+107insCTG
NM_001300984.2:c.-22+106_-22+107insCTG	NP_001287913.1:n.-22+106_-22+107insCTG