Canonical Allele Identifier: CA4061505
Gene: OPRM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 829214
ClinVar RCV Id: RCV001029133
dbSNP Id: rs9479757

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.154090209G>A , CM000668.2:g.154090209G>A GRCh38
NC_000006.11:g.154411344G>A , CM000668.1:g.154411344G>A GRCh37
NC_000006.10:g.154453037G>A NCBI36
NG_021208.1:g.84709G>A
NG_021208.2:g.84709G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000330432.12:c.643+31G>A MANE Select ENSP00000328264.7:p.=
ENST00000229768.9:c.643+31G>A ENSP00000229768.5:p.=
ENST00000330432.11:c.643+31G>A ENSP00000328264.7:p.=
ENST00000337049.8:c.643+31G>A ENSP00000338381.4:p.=
ENST00000360422.8:c.829+31G>A ENSP00000353598.5:p.=
ENST00000414028.6:c.643+31G>A ENSP00000399359.2:p.=
ENST00000419506.6:c.643+31G>A ENSP00000403549.2:p.=
ENST00000428397.6:c.643+31G>A ENSP00000411903.2:p.=
ENST00000434900.6:c.922+31G>A ENSP00000394624.2:p.=
ENST00000435918.6:c.643+31G>A ENSP00000413752.2:p.=
ENST00000452687.6:c.643+31G>A ENSP00000410497.2:p.=
ENST00000518759.5:c.400+31G>A ENSP00000430260.1:p.=
ENST00000519083.5:c.643+31G>A ENSP00000431048.1:p.=
ENST00000519613.5:n.575+31G>A
ENST00000520708.5:c.343+31G>A ENSP00000430876.1:p.=
ENST00000521106.1:n.353+31G>A
ENST00000522236.1:c.343+31G>A ENSP00000429373.1:p.=
ENST00000522382.1:n.417+31G>A
ENST00000522555.5:c.343+31G>A ENSP00000429719.1:p.=
ENST00000522739.5:c.643+31G>A ENSP00000428018.1:p.=
ENST00000524150.2:c.291-743G>A ENSP00000430575.1:p.=
ENST00000524163.5:c.643+31G>A ENSP00000430097.1:p.=
NM_000914.4:c.643+31G>A NP_000905.3:p.=
NM_001008503.2:c.643+31G>A NP_001008503.2:p.=
NM_001008504.3:c.643+31G>A NP_001008504.2:p.=
NM_001008505.2:c.643+31G>A NP_001008505.2:p.=
NM_001145279.3:c.922+31G>A NP_001138751.1:p.=
NM_001145280.3:c.343+31G>A NP_001138752.1:p.=
NM_001145281.2:c.400+31G>A NP_001138753.1:p.=
NM_001145282.2:c.643+31G>A NP_001138754.1:p.=
NM_001145283.2:c.643+31G>A NP_001138755.1:p.=
NM_001145284.3:c.643+31G>A NP_001138756.1:p.=
NM_001145285.2:c.643+31G>A NP_001138757.1:p.=
NM_001145286.2:c.643+31G>A NP_001138758.1:p.=
NM_001145287.2:c.343+31G>A NP_001138759.1:p.=
NM_001285522.1:c.291-28474G>A NP_001272451.1:p.=
NM_001285523.1:c.643+31G>A NP_001272452.1:p.=
NM_001285524.1:c.922+31G>A NP_001272453.1:p.=
NM_001285526.1:c.343+31G>A NP_001272455.1:p.=
NM_001285527.1:c.343+31G>A NP_001272456.1:p.=
NM_001285528.1:c.343+31G>A NP_001272457.1:p.=
NR_104348.1:n.777+31G>A
NR_104349.1:n.777+31G>A
NR_104350.1:n.425-743G>A
NR_104351.1:n.777+31G>A
XM_011535849.1:c.922+31G>A XP_011534151.1:p.=
XM_011535850.1:c.436+31G>A XP_011534152.1:p.=
XM_011535851.1:c.343+31G>A XP_011534153.1:p.=
XM_011535852.1:c.343+31G>A XP_011534154.1:p.=
XM_011535853.1:c.343+31G>A XP_011534155.1:p.=
XM_011535854.1:c.343+31G>A XP_011534156.1:p.=
XM_011535855.1:c.343+31G>A XP_011534157.1:p.=
XM_011535856.1:c.343+31G>A XP_011534158.1:p.=
XM_011535857.1:c.343+31G>A XP_011534159.1:p.=
XM_011535858.1:c.343+31G>A XP_011534160.1:p.=
XM_011535859.1:c.343+31G>A XP_011534161.1:p.=
XM_011535860.1:c.343+31G>A XP_011534162.1:p.=
XM_011535861.1:c.343+31G>A XP_011534163.1:p.=
XM_011535862.1:c.343+31G>A XP_011534164.1:p.=
NM_001285523.2:c.643+31G>A NP_001272452.1:p.=
NM_001285528.2:c.343+31G>A NP_001272457.1:p.=
XM_011535851.3:c.343+31G>A XP_011534153.1:p.=
XM_011535853.2:c.343+31G>A XP_011534155.1:p.=
XM_011535856.2:c.343+31G>A XP_011534158.1:p.=
XM_011535862.2:c.343+31G>A XP_011534164.1:p.=
XM_017010903.2:c.343+31G>A XP_016866392.1:p.=
XM_017010904.1:c.343+31G>A XP_016866393.1:p.=
XM_017010905.1:c.343+31G>A XP_016866394.1:p.=
XM_017010906.2:c.343+31G>A XP_016866395.1:p.=
NM_000914.5:c.643+31G>A MANE Select NP_000905.3:p.=
NM_001008503.3:c.643+31G>A NP_001008503.2:p.=
NM_001008504.4:c.643+31G>A NP_001008504.2:p.=
NM_001145279.4:c.922+31G>A NP_001138751.1:p.=
NM_001145280.4:c.343+31G>A NP_001138752.1:p.=
NM_001145281.3:c.400+31G>A NP_001138753.1:p.=
NM_001145285.3:c.643+31G>A NP_001138757.1:p.=
NM_001145286.3:c.643+31G>A NP_001138758.1:p.=
NM_001145287.3:c.343+31G>A NP_001138759.1:p.=
NM_001285523.3:c.643+31G>A NP_001272452.1:p.=
NM_001285526.2:c.343+31G>A NP_001272455.1:p.=