Canonical Allele Identifier: CA1674071643
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039541T= , CM000668.2:g.154039541T= GRCh38
NC_000006.11:g.154360676T= , CM000668.1:g.154360676T= GRCh37
NC_000006.10:g.154402369T= NCBI36
NG_021208.1:g.34041T=
NG_021208.2:g.34041T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-4T= MANE Select ENSP00000328264.7:n.-4T=
ENST00000229768.9:c.-4T= ENSP00000229768.5:n.-4T=
ENST00000330432.11:c.-4T= ENSP00000328264.7:n.-4T=
ENST00000337049.8:c.-4T= ENSP00000338381.4:n.-4T=
ENST00000360422.8:c.183T= ENSP00000353598.5:p.Ser61=
ENST00000414028.6:c.-4T= ENSP00000399359.2:n.-4T=
ENST00000419506.6:c.-4T= ENSP00000403549.2:n.-4T=
ENST00000428397.6:c.-4T= ENSP00000411903.2:n.-4T=
ENST00000434900.6:c.276T= ENSP00000394624.2:p.Ser92=
ENST00000435918.6:c.-4T= ENSP00000413752.2:n.-4T=
ENST00000452687.6:c.-4T= ENSP00000410497.2:n.-4T=
ENST00000518759.5:c.47+28982T= ENSP00000430260.1:n.47+28982T=
ENST00000519083.5:c.-4T= ENSP00000431048.1:n.-4T=
ENST00000520282.5:c.141T= ENSP00000430247.1:p.Ser47=
ENST00000520708.5:c.-11+28523T= ENSP00000430876.1:n.-11+28523T=
ENST00000522739.5:c.-4T= ENSP00000428018.1:n.-4T=
ENST00000523520.1:n.178T=
ENST00000524150.2:c.-4T= ENSP00000430575.1:n.-4T=
ENST00000524163.5:c.-4T= ENSP00000430097.1:n.-4T=
NM_000914.4:c.-4T= NP_000905.3:n.-4T=
NM_001008503.2:c.-4T= NP_001008503.2:n.-4T=
NM_001008504.3:c.-4T= NP_001008504.2:n.-4T=
NM_001008505.2:c.-4T= NP_001008505.2:n.-4T=
NM_001145279.3:c.276T= NP_001138751.1:p.Ser92=
NM_001145280.3:c.-11+28523T= NP_001138752.1:n.-11+28523T=
NM_001145281.2:c.47+28982T= NP_001138753.1:n.47+28982T=
NM_001145282.2:c.-4T= NP_001138754.1:n.-4T=
NM_001145283.2:c.-4T= NP_001138755.1:n.-4T=
NM_001145284.3:c.-4T= NP_001138756.1:n.-4T=
NM_001145285.2:c.-4T= NP_001138757.1:n.-4T=
NM_001145286.2:c.-4T= NP_001138758.1:n.-4T=
NM_001285522.1:c.-4T= NP_001272451.1:n.-4T=
NM_001285523.1:c.-4T= NP_001272452.1:n.-4T=
NM_001285524.1:c.276T= NP_001272453.1:p.Ser92=
NR_104348.1:n.131T=
NR_104349.1:n.131T=
NR_104350.1:n.131T=
NR_104351.1:n.131T=
XM_006715497.2:c.183T= XP_006715560.1:p.Ser61=
XM_011535849.1:c.276T= XP_011534151.1:p.Ser92=
NM_001285523.2:c.-4T= NP_001272452.1:n.-4T=
XM_017010907.2:c.183T= XP_016866396.1:p.Ser61=
NM_000914.5:c.-4T= MANE Select NP_000905.3:n.-4T=
NM_001008503.3:c.-4T= NP_001008503.2:n.-4T=
NM_001008504.4:c.-4T= NP_001008504.2:n.-4T=
NM_001145279.4:c.276T= NP_001138751.1:p.Ser92=
NM_001145280.4:c.-11+28523T= NP_001138752.1:n.-11+28523T=
NM_001145281.3:c.47+28982T= NP_001138753.1:n.47+28982T=
NM_001145285.3:c.-4T= NP_001138757.1:n.-4T=
NM_001145286.3:c.-4T= NP_001138758.1:n.-4T=
NM_001285523.3:c.-4T= NP_001272452.1:n.-4T=