Canonical Allele Identifier: CA1674071565
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039516_154039517delinsAC , CM000668.2:g.154039516_154039517delinsAC GRCh38
NC_000006.11:g.154360651_154360652delinsAC , CM000668.1:g.154360651_154360652delinsAC GRCh37
NC_000006.10:g.154402344_154402345delinsAC NCBI36
NG_021208.1:g.34016_34017delinsAC
NG_021208.2:g.34016_34017delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-29_-28delinsAC MANE Select ENSP00000328264.7:n.-29_-28delinsAC
ENST00000229768.9:c.-29_-28delinsAC ENSP00000229768.5:n.-29_-28delinsAC
ENST00000330432.11:c.-29_-28delinsAC ENSP00000328264.7:n.-29_-28delinsAC
ENST00000337049.8:c.-29_-28delinsAC ENSP00000338381.4:n.-29_-28delinsAC
ENST00000360422.8:c.158_159delinsAC ENSP00000353598.5:p.His53=
ENST00000414028.6:c.-29_-28delinsAC ENSP00000399359.2:n.-29_-28delinsAC
ENST00000419506.6:c.-29_-28delinsAC ENSP00000403549.2:n.-29_-28delinsAC
ENST00000428397.6:c.-29_-28delinsAC ENSP00000411903.2:n.-29_-28delinsAC
ENST00000434900.6:c.251_252delinsAC ENSP00000394624.2:p.His84=
ENST00000435918.6:c.-29_-28delinsAC ENSP00000413752.2:n.-29_-28delinsAC
ENST00000452687.6:c.-29_-28delinsAC ENSP00000410497.2:n.-29_-28delinsAC
ENST00000518759.5:c.47+28957_47+28958delinsAC ENSP00000430260.1:n.47+28957_47+28958delinsAC
ENST00000519083.5:c.-29_-28delinsAC ENSP00000431048.1:n.-29_-28delinsAC
ENST00000520282.5:c.116_117delinsAC ENSP00000430247.1:p.His39=
ENST00000520708.5:c.-11+28498_-11+28499delinsAC ENSP00000430876.1:n.-11+28498_-11+28499delinsAC
ENST00000522739.5:c.-29_-28delinsAC ENSP00000428018.1:n.-29_-28delinsAC
ENST00000523520.1:n.153_154delinsAC
ENST00000524150.2:c.-29_-28delinsAC ENSP00000430575.1:n.-29_-28delinsAC
ENST00000524163.5:c.-29_-28delinsAC ENSP00000430097.1:n.-29_-28delinsAC
NM_000914.4:c.-29_-28delinsAC NP_000905.3:n.-29_-28delinsAC
NM_001008503.2:c.-29_-28delinsAC NP_001008503.2:n.-29_-28delinsAC
NM_001008504.3:c.-29_-28delinsAC NP_001008504.2:n.-29_-28delinsAC
NM_001008505.2:c.-29_-28delinsAC NP_001008505.2:n.-29_-28delinsAC
NM_001145279.3:c.251_252delinsAC NP_001138751.1:p.His84=
NM_001145280.3:c.-11+28498_-11+28499delinsAC NP_001138752.1:n.-11+28498_-11+28499delinsAC
NM_001145281.2:c.47+28957_47+28958delinsAC NP_001138753.1:n.47+28957_47+28958delinsAC
NM_001145282.2:c.-29_-28delinsAC NP_001138754.1:n.-29_-28delinsAC
NM_001145283.2:c.-29_-28delinsAC NP_001138755.1:n.-29_-28delinsAC
NM_001145284.3:c.-29_-28delinsAC NP_001138756.1:n.-29_-28delinsAC
NM_001145285.2:c.-29_-28delinsAC NP_001138757.1:n.-29_-28delinsAC
NM_001145286.2:c.-29_-28delinsAC NP_001138758.1:n.-29_-28delinsAC
NM_001285522.1:c.-29_-28delinsAC NP_001272451.1:n.-29_-28delinsAC
NM_001285523.1:c.-29_-28delinsAC NP_001272452.1:n.-29_-28delinsAC
NM_001285524.1:c.251_252delinsAC NP_001272453.1:p.His84=
NR_104348.1:n.106_107delinsAC
NR_104349.1:n.106_107delinsAC
NR_104350.1:n.106_107delinsAC
NR_104351.1:n.106_107delinsAC
XM_006715497.2:c.158_159delinsAC XP_006715560.1:p.His53=
XM_011535849.1:c.251_252delinsAC XP_011534151.1:p.His84=
NM_001285523.2:c.-29_-28delinsAC NP_001272452.1:n.-29_-28delinsAC
XM_017010907.2:c.158_159delinsAC XP_016866396.1:p.His53=
NM_000914.5:c.-29_-28delinsAC MANE Select NP_000905.3:n.-29_-28delinsAC
NM_001008503.3:c.-29_-28delinsAC NP_001008503.2:n.-29_-28delinsAC
NM_001008504.4:c.-29_-28delinsAC NP_001008504.2:n.-29_-28delinsAC
NM_001145279.4:c.251_252delinsAC NP_001138751.1:p.His84=
NM_001145280.4:c.-11+28498_-11+28499delinsAC NP_001138752.1:n.-11+28498_-11+28499delinsAC
NM_001145281.3:c.47+28957_47+28958delinsAC NP_001138753.1:n.47+28957_47+28958delinsAC
NM_001145285.3:c.-29_-28delinsAC NP_001138757.1:n.-29_-28delinsAC
NM_001145286.3:c.-29_-28delinsAC NP_001138758.1:n.-29_-28delinsAC
NM_001285523.3:c.-29_-28delinsAC NP_001272452.1:n.-29_-28delinsAC