Canonical Allele Identifier: CA366152135

Gene: OPRM1

Linked Data

• ClinVar Variation Id: 829271
• ClinVar RCV Id: RCV001029192
• dbSNP Id: rs1465337438
• MyVariant Identifiers: chr6:g.154360609C>A (hg19) ; chr6:g.154039474C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039474C>A , CM000668.2:g.154039474C>A	GRCh38
NC_000006.11:g.154360609C>A , CM000668.1:g.154360609C>A	GRCh37
NC_000006.10:g.154402302C>A	NCBI36
NG_021208.1:g.33974C>A
NG_021208.2:g.33974C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000330432.12:c.-71C>A MANE Select	ENSP00000328264.7:n.-71C>A
ENST00000330432.11:c.-71C>A	ENSP00000328264.7:n.-71C>A
ENST00000360422.8:c.116C>A	ENSP00000353598.5:p.Ala39Glu
ENST00000428397.6:c.-71C>A	ENSP00000411903.2:n.-71C>A
ENST00000434900.6:c.209C>A	ENSP00000394624.2:p.Ala70Glu
ENST00000452687.6:c.-71C>A	ENSP00000410497.2:n.-71C>A
ENST00000518759.5:c.47+28915C>A	ENSP00000430260.1:n.47+28915C>A
ENST00000520282.5:c.74C>A	ENSP00000430247.1:p.Ala25Glu
ENST00000520708.5:c.-11+28456C>A	ENSP00000430876.1:n.-11+28456C>A
ENST00000523520.1:n.111C>A
NM_000914.4:c.-71C>A	NP_000905.3:n.-71C>A
NM_001008503.2:c.-71C>A	NP_001008503.2:n.-71C>A
NM_001008504.3:c.-71C>A	NP_001008504.2:n.-71C>A
NM_001008505.2:c.-71C>A	NP_001008505.2:n.-71C>A
NM_001145279.3:c.209C>A	NP_001138751.1:p.Ala70Glu
NM_001145280.3:c.-11+28456C>A	NP_001138752.1:n.-11+28456C>A
NM_001145281.2:c.47+28915C>A	NP_001138753.1:n.47+28915C>A
NM_001145282.2:c.-71C>A	NP_001138754.1:n.-71C>A
NM_001145283.2:c.-71C>A	NP_001138755.1:n.-71C>A
NM_001145284.3:c.-71C>A	NP_001138756.1:n.-71C>A
NM_001145285.2:c.-71C>A	NP_001138757.1:n.-71C>A
NM_001145286.2:c.-71C>A	NP_001138758.1:n.-71C>A
NM_001285522.1:c.-71C>A	NP_001272451.1:n.-71C>A
NM_001285523.1:c.-71C>A	NP_001272452.1:n.-71C>A
NM_001285524.1:c.209C>A	NP_001272453.1:p.Ala70Glu
NR_104348.1:n.64C>A
NR_104349.1:n.64C>A
NR_104350.1:n.64C>A
NR_104351.1:n.64C>A
XM_006715497.2:c.116C>A	XP_006715560.1:p.Ala39Glu
XM_011535849.1:c.209C>A	XP_011534151.1:p.Ala70Glu
NM_001285523.2:c.-71C>A	NP_001272452.1:n.-71C>A
XM_017010907.2:c.116C>A	XP_016866396.1:p.Ala39Glu
NM_000914.5:c.-71C>A MANE Select	NP_000905.3:n.-71C>A
NM_001008503.3:c.-71C>A	NP_001008503.2:n.-71C>A
NM_001008504.4:c.-71C>A	NP_001008504.2:n.-71C>A
NM_001145279.4:c.209C>A	NP_001138751.1:p.Ala70Glu
NM_001145280.4:c.-11+28456C>A	NP_001138752.1:n.-11+28456C>A
NM_001145281.3:c.47+28915C>A	NP_001138753.1:n.47+28915C>A
NM_001145285.3:c.-71C>A	NP_001138757.1:n.-71C>A
NM_001145286.3:c.-71C>A	NP_001138758.1:n.-71C>A
NM_001285523.3:c.-71C>A	NP_001272452.1:n.-71C>A