Canonical Allele Identifier: CA915944726

Gene: OPRM1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154107906T>C , CM000668.2:g.154107906T>C	GRCh38
NC_000006.11:g.154429041T>C , CM000668.1:g.154429041T>C	GRCh37
NC_000006.10:g.154470733T>C	NCBI36
NG_021208.1:g.102406T>C
NG_021208.2:g.102406T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000914.5:c.1165-10777T>C MANE Select	NP_000905.3:n.1165-10777T>C
ENST00000330432.12:c.1165-10777T>C MANE Select	ENSP00000328264.7:n.1165-10777T>C
NM_000914.4:c.1165-10777T>C	NP_000905.3:n.1165-10777T>C
NM_001008503.2:c.1164+16434T>C	NP_001008503.2:n.1164+16434T>C
NM_001008503.3:c.1164+16434T>C	NP_001008503.2:n.1164+16434T>C
NM_001145279.3:c.1444-10777T>C	NP_001138751.1:n.1444-10777T>C
NM_001145279.4:c.1444-10777T>C	NP_001138751.1:n.1444-10777T>C
NM_001145280.3:c.865-10777T>C	NP_001138752.1:n.865-10777T>C
NM_001145280.4:c.865-10777T>C	NP_001138752.1:n.865-10777T>C
NM_001145281.2:c.922-10777T>C	NP_001138753.1:n.922-10777T>C
NM_001145281.3:c.922-10777T>C	NP_001138753.1:n.922-10777T>C
NM_001145282.2:c.1165-2449T>C	NP_001138754.1:n.1165-2449T>C
NM_001145283.2:c.1165-110T>C	NP_001138755.1:n.1165-110T>C
NM_001145284.3:c.*111T>C	NP_001138756.1:n.*111T>C
NM_001145287.2:c.865-10777T>C	NP_001138759.1:n.865-10777T>C
NM_001145287.3:c.865-10777T>C	NP_001138759.1:n.865-10777T>C
NM_001285522.1:c.291-10777T>C	NP_001272451.1:n.291-10777T>C
NM_001285524.1:c.1444-10777T>C	NP_001272453.1:n.1444-10777T>C
NM_001285526.1:c.865-10777T>C	NP_001272455.1:n.865-10777T>C
NM_001285526.2:c.865-10777T>C	NP_001272455.1:n.865-10777T>C
NR_104348.1:n.1408-10777T>C
NR_104349.1:n.1408-2449T>C
NR_104350.1:n.946-10777T>C
NR_104351.1:n.1566T>C
ENST00000330432.11:c.1165-10777T>C	ENSP00000328264.7:n.1165-10777T>C
ENST00000337049.8:c.1164+16434T>C	ENSP00000338381.4:n.1164+16434T>C
ENST00000414028.6:c.*111T>C	ENSP00000399359.2:n.*111T>C
ENST00000434900.6:c.1444-10777T>C	ENSP00000394624.2:n.1444-10777T>C
ENST00000435918.6:c.1165-110T>C	ENSP00000413752.2:n.1165-110T>C
ENST00000452687.6:c.1165-2449T>C	ENSP00000410497.2:n.1165-2449T>C
ENST00000518759.5:c.922-10777T>C	ENSP00000430260.1:n.922-10777T>C
ENST00000519083.5:c.*223T>C	ENSP00000431048.1:n.*223T>C
ENST00000519613.5:n.1097-10777T>C
ENST00000520708.5:c.865-10777T>C	ENSP00000430876.1:n.865-10777T>C
ENST00000522236.1:c.865-10777T>C	ENSP00000429373.1:n.865-10777T>C
ENST00000522555.5:c.865-10777T>C	ENSP00000429719.1:n.865-10777T>C
ENST00000522739.5:c.*65-10777T>C	ENSP00000428018.1:n.*65-10777T>C
ENST00000524150.2:c.*250+16434T>C	ENSP00000430575.1:n.*250+16434T>C
XM_011535849.1:c.1444-10777T>C	XP_011534151.1:n.1444-10777T>C
XM_011535859.1:c.865-10777T>C	XP_011534161.1:n.865-10777T>C
XM_011535860.1:c.865-10777T>C	XP_011534162.1:n.865-10777T>C
XM_011535861.1:c.865-10777T>C	XP_011534163.1:n.865-10777T>C
XM_017010906.2:c.865-10777T>C	XP_016866395.1:n.865-10777T>C