Canonical Allele Identifier: CA1674071307

Gene: OPRM1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039391G= , CM000668.2:g.154039391G=	GRCh38
NC_000006.11:g.154360526G= , CM000668.1:g.154360526G=	GRCh37
NC_000006.10:g.154402219G=	NCBI36
NG_021208.1:g.33891G=
NG_021208.2:g.33891G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330432.12:c.-154G= MANE Select	ENSP00000328264.7:n.-154G=
ENST00000330432.11:c.-154G=	ENSP00000328264.7:n.-154G=
ENST00000360422.8:c.33G=	ENSP00000353598.5:p.Leu11=
ENST00000428397.6:c.-154G=	ENSP00000411903.2:n.-154G=
ENST00000434900.6:c.146-20G=	ENSP00000394624.2:n.146-20G=
ENST00000518759.5:c.47+28832G=	ENSP00000430260.1:n.47+28832G=
ENST00000520282.5:c.11-20G=	ENSP00000430247.1:n.11-20G=
ENST00000520708.5:c.-11+28373G=	ENSP00000430876.1:n.-11+28373G=
ENST00000523520.1:n.28G=
NM_000914.4:c.-154G=	NP_000905.3:n.-154G=
NM_001008504.3:c.-154G=	NP_001008504.2:n.-154G=
NM_001145279.3:c.146-20G=	NP_001138751.1:n.146-20G=
NM_001145280.3:c.-11+28373G=	NP_001138752.1:n.-11+28373G=
NM_001145281.2:c.47+28832G=	NP_001138753.1:n.47+28832G=
NM_001285522.1:c.-154G=	NP_001272451.1:n.-154G=
NM_001285523.1:c.-154G=	NP_001272452.1:n.-154G=
NM_001285524.1:c.146-20G=	NP_001272453.1:n.146-20G=
XM_006715497.2:c.33G=	XP_006715560.1:p.Leu11=
XM_011535849.1:c.146-20G=	XP_011534151.1:n.146-20G=
NM_001285523.2:c.-154G=	NP_001272452.1:n.-154G=
XM_017010907.2:c.33G=	XP_016866396.1:p.Leu11=
NM_000914.5:c.-154G= MANE Select	NP_000905.3:n.-154G=
NM_001008503.3:c.-154G=	NP_001008503.2:n.-154G=
NM_001008504.4:c.-154G=	NP_001008504.2:n.-154G=
NM_001145279.4:c.146-20G=	NP_001138751.1:n.146-20G=
NM_001145280.4:c.-11+28373G=	NP_001138752.1:n.-11+28373G=
NM_001145281.3:c.47+28832G=	NP_001138753.1:n.47+28832G=
NM_001145285.3:c.-154G=	NP_001138757.1:n.-154G=
NM_001145286.3:c.-154G=	NP_001138758.1:n.-154G=
NM_001285523.3:c.-154G=	NP_001272452.1:n.-154G=