Canonical Allele Identifier: CA1674066342
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154043277C= , CM000668.2:g.154043277C= GRCh38
NC_000006.11:g.154364412C= , CM000668.1:g.154364412C= GRCh37
NC_000006.10:g.154406105C= NCBI36
NG_021208.1:g.37777C=
NG_021208.2:g.37777C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.290+3443C= MANE Select ENSP00000328264.7:n.290+3443C=
ENST00000229768.9:c.290+3443C= ENSP00000229768.5:n.290+3443C=
ENST00000330432.11:c.290+3443C= ENSP00000328264.7:n.290+3443C=
ENST00000337049.8:c.290+3443C= ENSP00000338381.4:n.290+3443C=
ENST00000360422.8:c.476+3443C= ENSP00000353598.5:n.476+3443C=
ENST00000414028.6:c.290+3443C= ENSP00000399359.2:n.290+3443C=
ENST00000419506.6:c.290+3443C= ENSP00000403549.2:n.290+3443C=
ENST00000428397.6:c.290+3443C= ENSP00000411903.2:n.290+3443C=
ENST00000434900.6:c.569+3443C= ENSP00000394624.2:n.569+3443C=
ENST00000435918.6:c.290+3443C= ENSP00000413752.2:n.290+3443C=
ENST00000452687.6:c.290+3443C= ENSP00000410497.2:n.290+3443C=
ENST00000518759.5:c.47+32718C= ENSP00000430260.1:n.47+32718C=
ENST00000519083.5:c.290+3443C= ENSP00000431048.1:n.290+3443C=
ENST00000520282.5:c.434+3443C= ENSP00000430247.1:n.434+3443C=
ENST00000520708.5:c.-11+32259C= ENSP00000430876.1:n.-11+32259C=
ENST00000522739.5:c.290+3443C= ENSP00000428018.1:n.290+3443C=
ENST00000523520.1:n.472-3417C=
ENST00000524150.2:c.290+3443C= ENSP00000430575.1:n.290+3443C=
ENST00000524163.5:c.290+3443C= ENSP00000430097.1:n.290+3443C=
NM_000914.4:c.290+3443C= NP_000905.3:n.290+3443C=
NM_001008503.2:c.290+3443C= NP_001008503.2:n.290+3443C=
NM_001008504.3:c.290+3443C= NP_001008504.2:n.290+3443C=
NM_001008505.2:c.290+3443C= NP_001008505.2:n.290+3443C=
NM_001145279.3:c.569+3443C= NP_001138751.1:n.569+3443C=
NM_001145280.3:c.-11+32259C= NP_001138752.1:n.-11+32259C=
NM_001145281.2:c.47+32718C= NP_001138753.1:n.47+32718C=
NM_001145282.2:c.290+3443C= NP_001138754.1:n.290+3443C=
NM_001145283.2:c.290+3443C= NP_001138755.1:n.290+3443C=
NM_001145284.3:c.290+3443C= NP_001138756.1:n.290+3443C=
NM_001145285.2:c.290+3443C= NP_001138757.1:n.290+3443C=
NM_001145286.2:c.290+3443C= NP_001138758.1:n.290+3443C=
NM_001285522.1:c.290+3443C= NP_001272451.1:n.290+3443C=
NM_001285523.1:c.290+3443C= NP_001272452.1:n.290+3443C=
NM_001285524.1:c.569+3443C= NP_001272453.1:n.569+3443C=
NR_104348.1:n.424+3443C=
NR_104349.1:n.424+3443C=
NR_104350.1:n.424+3443C=
NR_104351.1:n.424+3443C=
XM_006715497.2:c.477-3417C= XP_006715560.1:n.477-3417C=
XM_011535849.1:c.569+3443C= XP_011534151.1:n.569+3443C=
NM_001285523.2:c.290+3443C= NP_001272452.1:n.290+3443C=
XM_017010907.2:c.476+3443C= XP_016866396.1:n.476+3443C=
NM_000914.5:c.290+3443C= MANE Select NP_000905.3:n.290+3443C=
NM_001008503.3:c.290+3443C= NP_001008503.2:n.290+3443C=
NM_001008504.4:c.290+3443C= NP_001008504.2:n.290+3443C=
NM_001145279.4:c.569+3443C= NP_001138751.1:n.569+3443C=
NM_001145280.4:c.-11+32259C= NP_001138752.1:n.-11+32259C=
NM_001145281.3:c.47+32718C= NP_001138753.1:n.47+32718C=
NM_001145285.3:c.290+3443C= NP_001138757.1:n.290+3443C=
NM_001145286.3:c.290+3443C= NP_001138758.1:n.290+3443C=
NM_001285523.3:c.290+3443C= NP_001272452.1:n.290+3443C=