Canonical Allele Identifier: CA2713452519
Gene: OPRM1 HGNC NCBI

Linked Data

dbSNP Id: rs2128394373

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039729_154039731dup , CM000668.2:g.154039729_154039731dup GRCh38
NC_000006.11:g.154360864_154360866dup , CM000668.1:g.154360864_154360866dup GRCh37
NC_000006.10:g.154402557_154402559dup NCBI36
NG_021208.1:g.34229_34231dup
NG_021208.2:g.34229_34231dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000330432.12:c.185_187dup MANE Select ENSP00000328264.7:p.Thr62_Gly63insAla
ENST00000229768.9:c.185_187dup ENSP00000229768.5:p.Thr62_Gly63insAla
ENST00000330432.11:c.185_187dup ENSP00000328264.7:p.Thr62_Gly63insAla
ENST00000337049.8:c.185_187dup ENSP00000338381.4:p.Thr62_Gly63insAla
ENST00000360422.8:c.371_373dup ENSP00000353598.5:p.Thr124_Gly125insAla
ENST00000414028.6:c.185_187dup ENSP00000399359.2:p.Thr62_Gly63insAla
ENST00000419506.6:c.185_187dup ENSP00000403549.2:p.Thr62_Gly63insAla
ENST00000428397.6:c.185_187dup ENSP00000411903.2:p.Thr62_Gly63insAla
ENST00000434900.6:c.464_466dup ENSP00000394624.2:p.Thr155_Gly156insAla
ENST00000435918.6:c.185_187dup ENSP00000413752.2:p.Thr62_Gly63insAla
ENST00000452687.6:c.185_187dup ENSP00000410497.2:p.Thr62_Gly63insAla
ENST00000518759.5:c.47+29170_47+29172dup ENSP00000430260.1:n.47+29170_47+29172dup
ENST00000519083.5:c.185_187dup ENSP00000431048.1:p.Thr62_Gly63insAla
ENST00000520282.5:c.329_331dup ENSP00000430247.1:p.Thr110_Gly111insAla
ENST00000520708.5:c.-11+28711_-11+28713dup ENSP00000430876.1:n.-11+28711_-11+28713dup
ENST00000522739.5:c.185_187dup ENSP00000428018.1:p.Thr62_Gly63insAla
ENST00000523520.1:n.366_368dup
ENST00000524150.2:c.185_187dup ENSP00000430575.1:p.Thr62_Gly63insAla
ENST00000524163.5:c.185_187dup ENSP00000430097.1:p.Thr62_Gly63insAla
NM_000914.4:c.185_187dup NP_000905.3:p.Thr62_Gly63insAla
NM_001008503.2:c.185_187dup NP_001008503.2:p.Thr62_Gly63insAla
NM_001008504.3:c.185_187dup NP_001008504.2:p.Thr62_Gly63insAla
NM_001008505.2:c.185_187dup NP_001008505.2:p.Thr62_Gly63insAla
NM_001145279.3:c.464_466dup NP_001138751.1:p.Thr155_Gly156insAla
NM_001145280.3:c.-11+28711_-11+28713dup NP_001138752.1:n.-11+28711_-11+28713dup
NM_001145281.2:c.47+29170_47+29172dup NP_001138753.1:n.47+29170_47+29172dup
NM_001145282.2:c.185_187dup NP_001138754.1:p.Thr62_Gly63insAla
NM_001145283.2:c.185_187dup NP_001138755.1:p.Thr62_Gly63insAla
NM_001145284.3:c.185_187dup NP_001138756.1:p.Thr62_Gly63insAla
NM_001145285.2:c.185_187dup NP_001138757.1:p.Thr62_Gly63insAla
NM_001145286.2:c.185_187dup NP_001138758.1:p.Thr62_Gly63insAla
NM_001285522.1:c.185_187dup NP_001272451.1:p.Thr62_Gly63insAla
NM_001285523.1:c.185_187dup NP_001272452.1:p.Thr62_Gly63insAla
NM_001285524.1:c.464_466dup NP_001272453.1:p.Thr155_Gly156insAla
NR_104348.1:n.319_321dup
NR_104349.1:n.319_321dup
NR_104350.1:n.319_321dup
NR_104351.1:n.319_321dup
XM_006715497.2:c.371_373dup XP_006715560.1:p.Thr124_Gly125insAla
XM_011535849.1:c.464_466dup XP_011534151.1:p.Thr155_Gly156insAla
NM_001285523.2:c.185_187dup NP_001272452.1:p.Thr62_Gly63insAla
XM_017010907.2:c.371_373dup XP_016866396.1:p.Thr124_Gly125insAla
NM_000914.5:c.185_187dup MANE Select NP_000905.3:p.Thr62_Gly63insAla
NM_001008503.3:c.185_187dup NP_001008503.2:p.Thr62_Gly63insAla
NM_001008504.4:c.185_187dup NP_001008504.2:p.Thr62_Gly63insAla
NM_001145279.4:c.464_466dup NP_001138751.1:p.Thr155_Gly156insAla
NM_001145280.4:c.-11+28711_-11+28713dup NP_001138752.1:n.-11+28711_-11+28713dup
NM_001145281.3:c.47+29170_47+29172dup NP_001138753.1:n.47+29170_47+29172dup
NM_001145285.3:c.185_187dup NP_001138757.1:p.Thr62_Gly63insAla
NM_001145286.3:c.185_187dup NP_001138758.1:p.Thr62_Gly63insAla
NM_001285523.3:c.185_187dup NP_001272452.1:p.Thr62_Gly63insAla