Canonical Allele Identifier: CA915944534

Gene: OPRM1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154118869C>T , CM000668.2:g.154118869C>T	GRCh38
NC_000006.11:g.154440004C>T , CM000668.1:g.154440004C>T	GRCh37
NC_000006.10:g.154481696C>T	NCBI36
NG_021208.1:g.113369C>T
NG_021208.2:g.113369C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000914.5:c.*148C>T MANE Select	NP_000905.3:n.*148C>T
ENST00000330432.12:c.*148C>T MANE Select	ENSP00000328264.7:n.*148C>T
NM_000914.4:c.*148C>T	NP_000905.3:n.*148C>T
NM_001008503.2:c.1164+27397C>T	NP_001008503.2:n.1164+27397C>T
NM_001008503.3:c.1164+27397C>T	NP_001008503.2:n.1164+27397C>T
NM_001145279.3:c.*148C>T	NP_001138751.1:n.*148C>T
NM_001145279.4:c.*148C>T	NP_001138751.1:n.*148C>T
NM_001145280.3:c.*148C>T	NP_001138752.1:n.*148C>T
NM_001145280.4:c.*148C>T	NP_001138752.1:n.*148C>T
NM_001145281.2:c.*148C>T	NP_001138753.1:n.*148C>T
NM_001145281.3:c.*148C>T	NP_001138753.1:n.*148C>T
NM_001145287.2:c.*148C>T	NP_001138759.1:n.*148C>T
NM_001145287.3:c.*148C>T	NP_001138759.1:n.*148C>T
NM_001285522.1:c.*183C>T	NP_001272451.1:n.*183C>T
NM_001285524.1:c.*148C>T	NP_001272453.1:n.*148C>T
NM_001285526.1:c.*148C>T	NP_001272455.1:n.*148C>T
NM_001285526.2:c.*148C>T	NP_001272455.1:n.*148C>T
NR_104348.1:n.1594C>T
NR_104350.1:n.1132C>T
ENST00000330432.11:c.*148C>T	ENSP00000328264.7:n.*148C>T
ENST00000337049.8:c.1164+27397C>T	ENSP00000338381.4:n.1164+27397C>T
ENST00000522236.1:c.*148C>T	ENSP00000429373.1:n.*148C>T
ENST00000522555.5:c.*148C>T	ENSP00000429719.1:n.*148C>T
ENST00000524150.2:c.*250+27397C>T	ENSP00000430575.1:n.*250+27397C>T
XM_011535849.1:c.*148C>T	XP_011534151.1:n.*148C>T
XM_011535859.1:c.*148C>T	XP_011534161.1:n.*148C>T
XM_011535860.1:c.*148C>T	XP_011534162.1:n.*148C>T
XM_011535861.1:c.*148C>T	XP_011534163.1:n.*148C>T
XM_017010906.2:c.*148C>T	XP_016866395.1:n.*148C>T