Canonical Allele Identifier: CA452974044
Gene: OPRM1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.154360808C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154039673C>T , CM000668.2:g.154039673C>T GRCh38
NC_000006.11:g.154360808C>T , CM000668.1:g.154360808C>T GRCh37
NC_000006.10:g.154402501C>T NCBI36
NG_021208.1:g.34173C>T
NG_021208.2:g.34173C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000330432.12:c.129C>T MANE Select ENSP00000328264.7:p.Asp43=
ENST00000229768.9:c.129C>T ENSP00000229768.5:p.Asp43=
ENST00000330432.11:c.129C>T ENSP00000328264.7:p.Asp43=
ENST00000337049.8:c.129C>T ENSP00000338381.4:p.Asp43=
ENST00000360422.8:c.315C>T ENSP00000353598.5:p.Asp105=
ENST00000414028.6:c.129C>T ENSP00000399359.2:p.Asp43=
ENST00000419506.6:c.129C>T ENSP00000403549.2:p.Asp43=
ENST00000428397.6:c.129C>T ENSP00000411903.2:p.Asp43=
ENST00000434900.6:c.408C>T ENSP00000394624.2:p.Asp136=
ENST00000435918.6:c.129C>T ENSP00000413752.2:p.Asp43=
ENST00000452687.6:c.129C>T ENSP00000410497.2:p.Asp43=
ENST00000518759.5:c.47+29114C>T ENSP00000430260.1:n.47+29114C>T
ENST00000519083.5:c.129C>T ENSP00000431048.1:p.Asp43=
ENST00000520282.5:c.273C>T ENSP00000430247.1:p.Asp91=
ENST00000520708.5:c.-11+28655C>T ENSP00000430876.1:n.-11+28655C>T
ENST00000522739.5:c.129C>T ENSP00000428018.1:p.Asp43=
ENST00000523520.1:n.310C>T
ENST00000524150.2:c.129C>T ENSP00000430575.1:p.Asp43=
ENST00000524163.5:c.129C>T ENSP00000430097.1:p.Asp43=
NM_000914.4:c.129C>T NP_000905.3:p.Asp43=
NM_001008503.2:c.129C>T NP_001008503.2:p.Asp43=
NM_001008504.3:c.129C>T NP_001008504.2:p.Asp43=
NM_001008505.2:c.129C>T NP_001008505.2:p.Asp43=
NM_001145279.3:c.408C>T NP_001138751.1:p.Asp136=
NM_001145280.3:c.-11+28655C>T NP_001138752.1:n.-11+28655C>T
NM_001145281.2:c.47+29114C>T NP_001138753.1:n.47+29114C>T
NM_001145282.2:c.129C>T NP_001138754.1:p.Asp43=
NM_001145283.2:c.129C>T NP_001138755.1:p.Asp43=
NM_001145284.3:c.129C>T NP_001138756.1:p.Asp43=
NM_001145285.2:c.129C>T NP_001138757.1:p.Asp43=
NM_001145286.2:c.129C>T NP_001138758.1:p.Asp43=
NM_001285522.1:c.129C>T NP_001272451.1:p.Asp43=
NM_001285523.1:c.129C>T NP_001272452.1:p.Asp43=
NM_001285524.1:c.408C>T NP_001272453.1:p.Asp136=
NR_104348.1:n.263C>T
NR_104349.1:n.263C>T
NR_104350.1:n.263C>T
NR_104351.1:n.263C>T
XM_006715497.2:c.315C>T XP_006715560.1:p.Asp105=
XM_011535849.1:c.408C>T XP_011534151.1:p.Asp136=
NM_001285523.2:c.129C>T NP_001272452.1:p.Asp43=
XM_017010907.2:c.315C>T XP_016866396.1:p.Asp105=
NM_000914.5:c.129C>T MANE Select NP_000905.3:p.Asp43=
NM_001008503.3:c.129C>T NP_001008503.2:p.Asp43=
NM_001008504.4:c.129C>T NP_001008504.2:p.Asp43=
NM_001145279.4:c.408C>T NP_001138751.1:p.Asp136=
NM_001145280.4:c.-11+28655C>T NP_001138752.1:n.-11+28655C>T
NM_001145281.3:c.47+29114C>T NP_001138753.1:n.47+29114C>T
NM_001145285.3:c.129C>T NP_001138757.1:p.Asp43=
NM_001145286.3:c.129C>T NP_001138758.1:p.Asp43=
NM_001285523.3:c.129C>T NP_001272452.1:p.Asp43=