Canonical Allele Identifier: CA2166468390

Gene: OCA2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28093420_28093425delinsAAAAAG , CM000677.2:g.28093420_28093425delinsAAAAAG	GRCh38
NC_000015.9:g.28338566_28338571delinsAAAAAG , CM000677.1:g.28338566_28338571delinsAAAAAG	GRCh37
NC_000015.8:g.26012161_26012166delinsAAAAAG	NCBI36
NG_009846.1:g.10888_10893delinsCTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000354638.8:c.-22+5799_-22+5804delinsCTTTTT MANE Select	ENSP00000346659.3:n.-22+5799_-22+5804delinsCTTTTT
ENST00000353809.9:c.-22+5799_-22+5804delinsCTTTTT	ENSP00000261276.8:n.-22+5799_-22+5804delinsCTTTTT
ENST00000354638.7:c.-22+5799_-22+5804delinsCTTTTT	ENSP00000346659.3:n.-22+5799_-22+5804delinsCTTTTT
ENST00000431101.1:c.-22+5686_-22+5691delinsCTTTTT	ENSP00000415431.1:n.-22+5686_-22+5691delinsCTTTTT
ENST00000445578.5:c.-22+5799_-22+5804delinsCTTTTT	ENSP00000414425.1:n.-22+5799_-22+5804delinsCTTTTT
NM_000275.2:c.-22+5799_-22+5804delinsCTTTTT	NP_000266.2:n.-22+5799_-22+5804delinsCTTTTT
NM_001300984.1:c.-22+5799_-22+5804delinsCTTTTT	NP_001287913.1:n.-22+5799_-22+5804delinsCTTTTT
XM_011521640.1:c.-22+5799_-22+5804delinsCTTTTT	XP_011519942.1:n.-22+5799_-22+5804delinsCTTTTT
XM_011521640.2:c.-22+5799_-22+5804delinsCTTTTT	XP_011519942.1:n.-22+5799_-22+5804delinsCTTTTT
NM_000275.3:c.-22+5799_-22+5804delinsCTTTTT MANE Select	NP_000266.2:n.-22+5799_-22+5804delinsCTTTTT
NM_001300984.2:c.-22+5799_-22+5804delinsCTTTTT	NP_001287913.1:n.-22+5799_-22+5804delinsCTTTTT