Canonical Allele Identifier: CA821047616
Gene: OPRM1 HGNC NCBI

Linked Data

dbSNP Id: rs1303960537

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154040803A>G , CM000668.2:g.154040803A>G GRCh38
NC_000006.11:g.154361938A>G , CM000668.1:g.154361938A>G GRCh37
NC_000006.10:g.154403631A>G NCBI36
NG_021208.1:g.35303A>G
NG_021208.2:g.35303A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000330432.12:c.290+969A>G MANE Select ENSP00000328264.7:n.290+969A>G
ENST00000229768.9:c.290+969A>G ENSP00000229768.5:n.290+969A>G
ENST00000330432.11:c.290+969A>G ENSP00000328264.7:n.290+969A>G
ENST00000337049.8:c.290+969A>G ENSP00000338381.4:n.290+969A>G
ENST00000360422.8:c.476+969A>G ENSP00000353598.5:n.476+969A>G
ENST00000414028.6:c.290+969A>G ENSP00000399359.2:n.290+969A>G
ENST00000419506.6:c.290+969A>G ENSP00000403549.2:n.290+969A>G
ENST00000428397.6:c.290+969A>G ENSP00000411903.2:n.290+969A>G
ENST00000434900.6:c.569+969A>G ENSP00000394624.2:n.569+969A>G
ENST00000435918.6:c.290+969A>G ENSP00000413752.2:n.290+969A>G
ENST00000452687.6:c.290+969A>G ENSP00000410497.2:n.290+969A>G
ENST00000518759.5:c.47+30244A>G ENSP00000430260.1:n.47+30244A>G
ENST00000519083.5:c.290+969A>G ENSP00000431048.1:n.290+969A>G
ENST00000520282.5:c.434+969A>G ENSP00000430247.1:n.434+969A>G
ENST00000520708.5:c.-11+29785A>G ENSP00000430876.1:n.-11+29785A>G
ENST00000522739.5:c.290+969A>G ENSP00000428018.1:n.290+969A>G
ENST00000523520.1:n.471+969A>G
ENST00000524150.2:c.290+969A>G ENSP00000430575.1:n.290+969A>G
ENST00000524163.5:c.290+969A>G ENSP00000430097.1:n.290+969A>G
NM_000914.4:c.290+969A>G NP_000905.3:n.290+969A>G
NM_001008503.2:c.290+969A>G NP_001008503.2:n.290+969A>G
NM_001008504.3:c.290+969A>G NP_001008504.2:n.290+969A>G
NM_001008505.2:c.290+969A>G NP_001008505.2:n.290+969A>G
NM_001145279.3:c.569+969A>G NP_001138751.1:n.569+969A>G
NM_001145280.3:c.-11+29785A>G NP_001138752.1:n.-11+29785A>G
NM_001145281.2:c.47+30244A>G NP_001138753.1:n.47+30244A>G
NM_001145282.2:c.290+969A>G NP_001138754.1:n.290+969A>G
NM_001145283.2:c.290+969A>G NP_001138755.1:n.290+969A>G
NM_001145284.3:c.290+969A>G NP_001138756.1:n.290+969A>G
NM_001145285.2:c.290+969A>G NP_001138757.1:n.290+969A>G
NM_001145286.2:c.290+969A>G NP_001138758.1:n.290+969A>G
NM_001285522.1:c.290+969A>G NP_001272451.1:n.290+969A>G
NM_001285523.1:c.290+969A>G NP_001272452.1:n.290+969A>G
NM_001285524.1:c.569+969A>G NP_001272453.1:n.569+969A>G
NR_104348.1:n.424+969A>G
NR_104349.1:n.424+969A>G
NR_104350.1:n.424+969A>G
NR_104351.1:n.424+969A>G
XM_006715497.2:c.476+969A>G XP_006715560.1:n.476+969A>G
XM_011535849.1:c.569+969A>G XP_011534151.1:n.569+969A>G
NM_001285523.2:c.290+969A>G NP_001272452.1:n.290+969A>G
XM_017010907.2:c.476+969A>G XP_016866396.1:n.476+969A>G
NM_000914.5:c.290+969A>G MANE Select NP_000905.3:n.290+969A>G
NM_001008503.3:c.290+969A>G NP_001008503.2:n.290+969A>G
NM_001008504.4:c.290+969A>G NP_001008504.2:n.290+969A>G
NM_001145279.4:c.569+969A>G NP_001138751.1:n.569+969A>G
NM_001145280.4:c.-11+29785A>G NP_001138752.1:n.-11+29785A>G
NM_001145281.3:c.47+30244A>G NP_001138753.1:n.47+30244A>G
NM_001145285.3:c.290+969A>G NP_001138757.1:n.290+969A>G
NM_001145286.3:c.290+969A>G NP_001138758.1:n.290+969A>G
NM_001285523.3:c.290+969A>G NP_001272452.1:n.290+969A>G