Canonical Allele Identifier: CA150238313

Gene: OPRM1

Linked Data

• dbSNP Id: rs201738594
• gnomAD v4: 6-154039294-G-C
• MyVariant Identifiers: chr6:g.154360429G>C (hg19) ; chr6:g.154039294G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039294G>C , CM000668.2:g.154039294G>C	GRCh38
NC_000006.11:g.154360429G>C , CM000668.1:g.154360429G>C	GRCh37
NC_000006.10:g.154402122G>C	NCBI36
NG_021208.1:g.33794G>C
NG_021208.2:g.33794G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330432.12:c.-251G>C MANE Select	ENSP00000328264.7:n.-251G>C
ENST00000360422.8:c.-65G>C	ENSP00000353598.5:n.-65G>C
ENST00000434900.6:c.134G>C	ENSP00000394624.2:p.Arg45Pro
ENST00000518759.5:c.47+28735G>C	ENSP00000430260.1:n.47+28735G>C
ENST00000520282.5:c.11-117G>C	ENSP00000430247.1:n.11-117G>C
ENST00000520708.5:c.-11+28276G>C	ENSP00000430876.1:n.-11+28276G>C
NM_000914.4:c.-251G>C	NP_000905.3:n.-251G>C
NM_001008504.3:c.-251G>C	NP_001008504.2:n.-251G>C
NM_001145279.3:c.134G>C	NP_001138751.1:p.Arg45Pro
NM_001145280.3:c.-11+28276G>C	NP_001138752.1:n.-11+28276G>C
NM_001145281.2:c.47+28735G>C	NP_001138753.1:n.47+28735G>C
NM_001285522.1:c.-251G>C	NP_001272451.1:n.-251G>C
NM_001285523.1:c.-251G>C	NP_001272452.1:n.-251G>C
NM_001285524.1:c.134G>C	NP_001272453.1:p.Arg45Pro
XM_006715497.2:c.-65G>C	XP_006715560.1:n.-65G>C
XM_011535849.1:c.134G>C	XP_011534151.1:p.Arg45Pro
NM_001285523.2:c.-251G>C	NP_001272452.1:n.-251G>C
XM_017010907.2:c.-65G>C	XP_016866396.1:n.-65G>C
NM_000914.5:c.-251G>C MANE Select	NP_000905.3:n.-251G>C
NM_001008503.3:c.-251G>C	NP_001008503.2:n.-251G>C
NM_001008504.4:c.-251G>C	NP_001008504.2:n.-251G>C
NM_001145279.4:c.134G>C	NP_001138751.1:p.Arg45Pro
NM_001145280.4:c.-11+28276G>C	NP_001138752.1:n.-11+28276G>C
NM_001145281.3:c.47+28735G>C	NP_001138753.1:n.47+28735G>C
NM_001145285.3:c.-251G>C	NP_001138757.1:n.-251G>C
NM_001145286.3:c.-251G>C	NP_001138758.1:n.-251G>C
NM_001285523.3:c.-251G>C	NP_001272452.1:n.-251G>C