Canonical Allele Identifier: CA1784495356

Gene: OPRK1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.53229597T= , CM000670.2:g.53229597T=	GRCh38
NC_000008.10:g.54142157T= , CM000670.1:g.54142157T=	GRCh37
NC_000008.9:g.54304710T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265572.8:c.843A= MANE Select	ENSP00000265572.3:p.Ala281=
ENST00000673285.2:c.843A=	ENSP00000500765.2:p.Ala281=
ENST00000265572.7:c.843A=	ENSP00000265572.3:p.Ala281=
ENST00000520287.5:c.843A=	ENSP00000429706.1:p.Ala281=
ENST00000522508.1:c.*666A=	ENSP00000428231.1:n.*666A=
ENST00000524278.5:c.576A=	ENSP00000430923.1:p.Ala192=
ENST00000612786.4:c.576A=	ENSP00000483000.1:p.Ala192=
ENST00000613482.1:c.801A=	ENSP00000478453.1:p.Ala267=
NM_000912.3:c.843A=	NP_000903.2:p.Ala281=
NM_001282904.1:c.576A=	NP_001269833.1:p.Ala192=
NM_000912.4:c.843A=	NP_000903.2:p.Ala281=
NM_001318497.1:c.843A=	NP_001305426.1:p.Ala281=
NM_000912.5:c.843A= MANE Select	NP_000903.2:p.Ala281=
NM_001318497.2:c.843A=	NP_001305426.1:p.Ala281=
NM_001282904.2:c.576A=	NP_001269833.1:p.Ala192=