Canonical Allele Identifier: CA366152236

Gene: OPRM1

Linked Data

• COSMIC: COSM3948295
• MyVariant Identifiers: chr6:g.154360668G>T (hg19) ; chr6:g.154039533G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039533G>T , CM000668.2:g.154039533G>T	GRCh38
NC_000006.11:g.154360668G>T , CM000668.1:g.154360668G>T	GRCh37
NC_000006.10:g.154402361G>T	NCBI36
NG_021208.1:g.34033G>T
NG_021208.2:g.34033G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330432.12:c.-12G>T MANE Select	ENSP00000328264.7:n.-12G>T
ENST00000229768.9:c.-12G>T	ENSP00000229768.5:n.-12G>T
ENST00000330432.11:c.-12G>T	ENSP00000328264.7:n.-12G>T
ENST00000337049.8:c.-12G>T	ENSP00000338381.4:n.-12G>T
ENST00000360422.8:c.175G>T	ENSP00000353598.5:p.Ala59Ser
ENST00000414028.6:c.-12G>T	ENSP00000399359.2:n.-12G>T
ENST00000419506.6:c.-12G>T	ENSP00000403549.2:n.-12G>T
ENST00000428397.6:c.-12G>T	ENSP00000411903.2:n.-12G>T
ENST00000434900.6:c.268G>T	ENSP00000394624.2:p.Ala90Ser
ENST00000435918.6:c.-12G>T	ENSP00000413752.2:n.-12G>T
ENST00000452687.6:c.-12G>T	ENSP00000410497.2:n.-12G>T
ENST00000518759.5:c.47+28974G>T	ENSP00000430260.1:n.47+28974G>T
ENST00000519083.5:c.-12G>T	ENSP00000431048.1:n.-12G>T
ENST00000520282.5:c.133G>T	ENSP00000430247.1:p.Ala45Ser
ENST00000520708.5:c.-11+28515G>T	ENSP00000430876.1:n.-11+28515G>T
ENST00000522739.5:c.-12G>T	ENSP00000428018.1:n.-12G>T
ENST00000523520.1:n.170G>T
ENST00000524150.2:c.-12G>T	ENSP00000430575.1:n.-12G>T
ENST00000524163.5:c.-12G>T	ENSP00000430097.1:n.-12G>T
NM_000914.4:c.-12G>T	NP_000905.3:n.-12G>T
NM_001008503.2:c.-12G>T	NP_001008503.2:n.-12G>T
NM_001008504.3:c.-12G>T	NP_001008504.2:n.-12G>T
NM_001008505.2:c.-12G>T	NP_001008505.2:n.-12G>T
NM_001145279.3:c.268G>T	NP_001138751.1:p.Ala90Ser
NM_001145280.3:c.-11+28515G>T	NP_001138752.1:n.-11+28515G>T
NM_001145281.2:c.47+28974G>T	NP_001138753.1:n.47+28974G>T
NM_001145282.2:c.-12G>T	NP_001138754.1:n.-12G>T
NM_001145283.2:c.-12G>T	NP_001138755.1:n.-12G>T
NM_001145284.3:c.-12G>T	NP_001138756.1:n.-12G>T
NM_001145285.2:c.-12G>T	NP_001138757.1:n.-12G>T
NM_001145286.2:c.-12G>T	NP_001138758.1:n.-12G>T
NM_001285522.1:c.-12G>T	NP_001272451.1:n.-12G>T
NM_001285523.1:c.-12G>T	NP_001272452.1:n.-12G>T
NM_001285524.1:c.268G>T	NP_001272453.1:p.Ala90Ser
NR_104348.1:n.123G>T
NR_104349.1:n.123G>T
NR_104350.1:n.123G>T
NR_104351.1:n.123G>T
XM_006715497.2:c.175G>T	XP_006715560.1:p.Ala59Ser
XM_011535849.1:c.268G>T	XP_011534151.1:p.Ala90Ser
NM_001285523.2:c.-12G>T	NP_001272452.1:n.-12G>T
XM_017010907.2:c.175G>T	XP_016866396.1:p.Ala59Ser
NM_000914.5:c.-12G>T MANE Select	NP_000905.3:n.-12G>T
NM_001008503.3:c.-12G>T	NP_001008503.2:n.-12G>T
NM_001008504.4:c.-12G>T	NP_001008504.2:n.-12G>T
NM_001145279.4:c.268G>T	NP_001138751.1:p.Ala90Ser
NM_001145280.4:c.-11+28515G>T	NP_001138752.1:n.-11+28515G>T
NM_001145281.3:c.47+28974G>T	NP_001138753.1:n.47+28974G>T
NM_001145285.3:c.-12G>T	NP_001138757.1:n.-12G>T
NM_001145286.3:c.-12G>T	NP_001138758.1:n.-12G>T
NM_001285523.3:c.-12G>T	NP_001272452.1:n.-12G>T