Canonical Allele Identifier: CA915944490

Gene: OPRM1

Linked Data

• ClinVar Variation Id: 828475
• ClinVar RCV Id: RCV001028385
• dbSNP Id: rs1583170107
• gnomAD v4: 6-154039336-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039336G>T , CM000668.2:g.154039336G>T	GRCh38
NC_000006.11:g.154360471G>T , CM000668.1:g.154360471G>T	GRCh37
NC_000006.10:g.154402164G>T	NCBI36
NG_021208.1:g.33836G>T
NG_021208.2:g.33836G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330432.12:c.-209G>T MANE Select	ENSP00000328264.7:n.-209G>T
ENST00000330432.11:c.-209G>T	ENSP00000328264.7:n.-209G>T
ENST00000360422.8:c.-23G>T	ENSP00000353598.5:n.-23G>T
ENST00000434900.6:c.145+31G>T	ENSP00000394624.2:n.145+31G>T
ENST00000518759.5:c.47+28777G>T	ENSP00000430260.1:n.47+28777G>T
ENST00000520282.5:c.11-75G>T	ENSP00000430247.1:n.11-75G>T
ENST00000520708.5:c.-11+28318G>T	ENSP00000430876.1:n.-11+28318G>T
NM_000914.4:c.-209G>T	NP_000905.3:n.-209G>T
NM_001008504.3:c.-209G>T	NP_001008504.2:n.-209G>T
NM_001145279.3:c.145+31G>T	NP_001138751.1:n.145+31G>T
NM_001145280.3:c.-11+28318G>T	NP_001138752.1:n.-11+28318G>T
NM_001145281.2:c.47+28777G>T	NP_001138753.1:n.47+28777G>T
NM_001285522.1:c.-209G>T	NP_001272451.1:n.-209G>T
NM_001285523.1:c.-209G>T	NP_001272452.1:n.-209G>T
NM_001285524.1:c.145+31G>T	NP_001272453.1:n.145+31G>T
XM_006715497.2:c.-23G>T	XP_006715560.1:n.-23G>T
XM_011535849.1:c.145+31G>T	XP_011534151.1:n.145+31G>T
NM_001285523.2:c.-209G>T	NP_001272452.1:n.-209G>T
XM_017010907.2:c.-23G>T	XP_016866396.1:n.-23G>T
NM_000914.5:c.-209G>T MANE Select	NP_000905.3:n.-209G>T
NM_001008503.3:c.-209G>T	NP_001008503.2:n.-209G>T
NM_001008504.4:c.-209G>T	NP_001008504.2:n.-209G>T
NM_001145279.4:c.145+31G>T	NP_001138751.1:n.145+31G>T
NM_001145280.4:c.-11+28318G>T	NP_001138752.1:n.-11+28318G>T
NM_001145281.3:c.47+28777G>T	NP_001138753.1:n.47+28777G>T
NM_001145285.3:c.-209G>T	NP_001138757.1:n.-209G>T
NM_001145286.3:c.-209G>T	NP_001138758.1:n.-209G>T
NM_001285523.3:c.-209G>T	NP_001272452.1:n.-209G>T