Canonical Allele Identifier: CA1674071271
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039378G= , CM000668.2:g.154039378G= GRCh38
NC_000006.11:g.154360513G= , CM000668.1:g.154360513G= GRCh37
NC_000006.10:g.154402206G= NCBI36
NG_021208.1:g.33878G=
NG_021208.2:g.33878G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-167G= MANE Select ENSP00000328264.7:n.-167G=
ENST00000330432.11:c.-167G= ENSP00000328264.7:n.-167G=
ENST00000360422.8:c.20G= ENSP00000353598.5:p.Gly7=
ENST00000428397.6:c.-167G= ENSP00000411903.2:n.-167G=
ENST00000434900.6:c.146-33G= ENSP00000394624.2:n.146-33G=
ENST00000518759.5:c.47+28819G= ENSP00000430260.1:n.47+28819G=
ENST00000520282.5:c.11-33G= ENSP00000430247.1:n.11-33G=
ENST00000520708.5:c.-11+28360G= ENSP00000430876.1:n.-11+28360G=
ENST00000523520.1:n.15G=
NM_000914.4:c.-167G= NP_000905.3:n.-167G=
NM_001008504.3:c.-167G= NP_001008504.2:n.-167G=
NM_001145279.3:c.146-33G= NP_001138751.1:n.146-33G=
NM_001145280.3:c.-11+28360G= NP_001138752.1:n.-11+28360G=
NM_001145281.2:c.47+28819G= NP_001138753.1:n.47+28819G=
NM_001285522.1:c.-167G= NP_001272451.1:n.-167G=
NM_001285523.1:c.-167G= NP_001272452.1:n.-167G=
NM_001285524.1:c.146-33G= NP_001272453.1:n.146-33G=
XM_006715497.2:c.20G= XP_006715560.1:p.Gly7=
XM_011535849.1:c.146-33G= XP_011534151.1:n.146-33G=
NM_001285523.2:c.-167G= NP_001272452.1:n.-167G=
XM_017010907.2:c.20G= XP_016866396.1:p.Gly7=
NM_000914.5:c.-167G= MANE Select NP_000905.3:n.-167G=
NM_001008503.3:c.-167G= NP_001008503.2:n.-167G=
NM_001008504.4:c.-167G= NP_001008504.2:n.-167G=
NM_001145279.4:c.146-33G= NP_001138751.1:n.146-33G=
NM_001145280.4:c.-11+28360G= NP_001138752.1:n.-11+28360G=
NM_001145281.3:c.47+28819G= NP_001138753.1:n.47+28819G=
NM_001145285.3:c.-167G= NP_001138757.1:n.-167G=
NM_001145286.3:c.-167G= NP_001138758.1:n.-167G=
NM_001285523.3:c.-167G= NP_001272452.1:n.-167G=