Canonical Allele Identifier: CA2166464882

Gene: OCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28090822_28090823delinsGA , CM000677.2:g.28090822_28090823delinsGA	GRCh38
NC_000015.9:g.28335968_28335969delinsGA , CM000677.1:g.28335968_28335969delinsGA	GRCh37
NC_000015.8:g.26009563_26009564delinsGA	NCBI36
NG_009846.1:g.13490_13491delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354638.8:c.-22+8401_-22+8402delinsTC MANE Select	ENSP00000346659.3:n.-22+8401_-22+8402delinsTC
ENST00000353809.9:c.-22+8401_-22+8402delinsTC	ENSP00000261276.8:n.-22+8401_-22+8402delinsTC
ENST00000354638.7:c.-22+8401_-22+8402delinsTC	ENSP00000346659.3:n.-22+8401_-22+8402delinsTC
ENST00000431101.1:c.-22+8288_-22+8289delinsTC	ENSP00000415431.1:n.-22+8288_-22+8289delinsTC
ENST00000445578.5:c.-22+8401_-22+8402delinsTC	ENSP00000414425.1:n.-22+8401_-22+8402delinsTC
NM_000275.2:c.-22+8401_-22+8402delinsTC	NP_000266.2:n.-22+8401_-22+8402delinsTC
NM_001300984.1:c.-22+8401_-22+8402delinsTC	NP_001287913.1:n.-22+8401_-22+8402delinsTC
XM_011521640.1:c.-22+8401_-22+8402delinsTC	XP_011519942.1:n.-22+8401_-22+8402delinsTC
XM_011521640.2:c.-22+8401_-22+8402delinsTC	XP_011519942.1:n.-22+8401_-22+8402delinsTC
NM_000275.3:c.-22+8401_-22+8402delinsTC MANE Select	NP_000266.2:n.-22+8401_-22+8402delinsTC
NM_001300984.2:c.-22+8401_-22+8402delinsTC	NP_001287913.1:n.-22+8401_-22+8402delinsTC