Canonical Allele Identifier: CA1674071284
Gene: OPRM1 HGNC NCBI

Linked Data

dbSNP Id: rs1779547685

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039383del , CM000668.2:g.154039383del GRCh38
NC_000006.11:g.154360518del , CM000668.1:g.154360518del GRCh37
NC_000006.10:g.154402211del NCBI36
NG_021208.1:g.33883del
NG_021208.2:g.33883del

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-162del MANE Select ENSP00000328264.7:n.-162del
ENST00000330432.11:c.-162del ENSP00000328264.7:n.-162del
ENST00000360422.8:c.25del ENSP00000353598.5:p.Leu9SerfsTer3
ENST00000428397.6:c.-162del ENSP00000411903.2:n.-162del
ENST00000434900.6:c.146-28del ENSP00000394624.2:n.146-28del
ENST00000518759.5:c.47+28824del ENSP00000430260.1:n.47+28824del
ENST00000520282.5:c.11-28del ENSP00000430247.1:n.11-28del
ENST00000520708.5:c.-11+28365del ENSP00000430876.1:n.-11+28365del
ENST00000523520.1:n.20del
NM_000914.4:c.-162del NP_000905.3:n.-162del
NM_001008504.3:c.-162del NP_001008504.2:n.-162del
NM_001145279.3:c.146-28del NP_001138751.1:n.146-28del
NM_001145280.3:c.-11+28365del NP_001138752.1:n.-11+28365del
NM_001145281.2:c.47+28824del NP_001138753.1:n.47+28824del
NM_001285522.1:c.-162del NP_001272451.1:n.-162del
NM_001285523.1:c.-162del NP_001272452.1:n.-162del
NM_001285524.1:c.146-28del NP_001272453.1:n.146-28del
XM_006715497.2:c.25del XP_006715560.1:p.Leu9SerfsTer3
XM_011535849.1:c.146-28del XP_011534151.1:n.146-28del
NM_001285523.2:c.-162del NP_001272452.1:n.-162del
XM_017010907.2:c.25del XP_016866396.1:p.Leu9SerfsTer3
NM_000914.5:c.-162del MANE Select NP_000905.3:n.-162del
NM_001008503.3:c.-162del NP_001008503.2:n.-162del
NM_001008504.4:c.-162del NP_001008504.2:n.-162del
NM_001145279.4:c.146-28del NP_001138751.1:n.146-28del
NM_001145280.4:c.-11+28365del NP_001138752.1:n.-11+28365del
NM_001145281.3:c.47+28824del NP_001138753.1:n.47+28824del
NM_001145285.3:c.-162del NP_001138757.1:n.-162del
NM_001145286.3:c.-162del NP_001138758.1:n.-162del
NM_001285523.3:c.-162del NP_001272452.1:n.-162del