Canonical Allele Identifier: CA2840239869
Gene: OPRM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039403dup , CM000668.2:g.154039403dup GRCh38
NC_000006.11:g.154360538dup , CM000668.1:g.154360538dup GRCh37
NC_000006.10:g.154402231dup NCBI36
NG_021208.1:g.33903dup
NG_021208.2:g.33903dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.-142dup MANE Select ENSP00000328264.7:n.-142dup
ENST00000330432.11:c.-142dup ENSP00000328264.7:n.-142dup
ENST00000360422.8:c.45dup ENSP00000353598.5:p.Val16CysfsTer9
ENST00000428397.6:c.-142dup ENSP00000411903.2:n.-142dup
ENST00000434900.6:c.146-8dup ENSP00000394624.2:n.146-8dup
ENST00000518759.5:c.47+28844dup ENSP00000430260.1:n.47+28844dup
ENST00000520282.5:c.11-8dup ENSP00000430247.1:n.11-8dup
ENST00000520708.5:c.-11+28385dup ENSP00000430876.1:n.-11+28385dup
ENST00000523520.1:n.40dup
NM_000914.4:c.-142dup NP_000905.3:n.-142dup
NM_001008504.3:c.-142dup NP_001008504.2:n.-142dup
NM_001145279.3:c.146-8dup NP_001138751.1:n.146-8dup
NM_001145280.3:c.-11+28385dup NP_001138752.1:n.-11+28385dup
NM_001145281.2:c.47+28844dup NP_001138753.1:n.47+28844dup
NM_001285522.1:c.-142dup NP_001272451.1:n.-142dup
NM_001285523.1:c.-142dup NP_001272452.1:n.-142dup
NM_001285524.1:c.146-8dup NP_001272453.1:n.146-8dup
XM_006715497.2:c.45dup XP_006715560.1:p.Val16CysfsTer9
XM_011535849.1:c.146-8dup XP_011534151.1:n.146-8dup
NM_001285523.2:c.-142dup NP_001272452.1:n.-142dup
XM_017010907.2:c.45dup XP_016866396.1:p.Val16CysfsTer9
NM_000914.5:c.-142dup MANE Select NP_000905.3:n.-142dup
NM_001008503.3:c.-142dup NP_001008503.2:n.-142dup
NM_001008504.4:c.-142dup NP_001008504.2:n.-142dup
NM_001145279.4:c.146-8dup NP_001138751.1:n.146-8dup
NM_001145280.4:c.-11+28385dup NP_001138752.1:n.-11+28385dup
NM_001145281.3:c.47+28844dup NP_001138753.1:n.47+28844dup
NM_001145285.3:c.-142dup NP_001138757.1:n.-142dup
NM_001145286.3:c.-142dup NP_001138758.1:n.-142dup
NM_001285523.3:c.-142dup NP_001272452.1:n.-142dup