Canonical Allele Identifier: CA366152312

Gene: OPRM1

Linked Data

• MyVariant Identifiers: chr6:g.154360704A>T (hg19) ; chr6:g.154039569A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039569A>T , CM000668.2:g.154039569A>T	GRCh38
NC_000006.11:g.154360704A>T , CM000668.1:g.154360704A>T	GRCh37
NC_000006.10:g.154402397A>T	NCBI36
NG_021208.1:g.34069A>T
NG_021208.2:g.34069A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330432.12:c.25A>T MANE Select	ENSP00000328264.7:p.Asn9Tyr
ENST00000229768.9:c.25A>T	ENSP00000229768.5:p.Asn9Tyr
ENST00000330432.11:c.25A>T	ENSP00000328264.7:p.Asn9Tyr
ENST00000337049.8:c.25A>T	ENSP00000338381.4:p.Asn9Tyr
ENST00000360422.8:c.211A>T	ENSP00000353598.5:p.Asn71Tyr
ENST00000414028.6:c.25A>T	ENSP00000399359.2:p.Asn9Tyr
ENST00000419506.6:c.25A>T	ENSP00000403549.2:p.Asn9Tyr
ENST00000428397.6:c.25A>T	ENSP00000411903.2:p.Asn9Tyr
ENST00000434900.6:c.304A>T	ENSP00000394624.2:p.Asn102Tyr
ENST00000435918.6:c.25A>T	ENSP00000413752.2:p.Asn9Tyr
ENST00000452687.6:c.25A>T	ENSP00000410497.2:p.Asn9Tyr
ENST00000518759.5:c.47+29010A>T	ENSP00000430260.1:n.47+29010A>T
ENST00000519083.5:c.25A>T	ENSP00000431048.1:p.Asn9Tyr
ENST00000520282.5:c.169A>T	ENSP00000430247.1:p.Asn57Tyr
ENST00000520708.5:c.-11+28551A>T	ENSP00000430876.1:n.-11+28551A>T
ENST00000522739.5:c.25A>T	ENSP00000428018.1:p.Asn9Tyr
ENST00000523520.1:n.206A>T
ENST00000524150.2:c.25A>T	ENSP00000430575.1:p.Asn9Tyr
ENST00000524163.5:c.25A>T	ENSP00000430097.1:p.Asn9Tyr
NM_000914.4:c.25A>T	NP_000905.3:p.Asn9Tyr
NM_001008503.2:c.25A>T	NP_001008503.2:p.Asn9Tyr
NM_001008504.3:c.25A>T	NP_001008504.2:p.Asn9Tyr
NM_001008505.2:c.25A>T	NP_001008505.2:p.Asn9Tyr
NM_001145279.3:c.304A>T	NP_001138751.1:p.Asn102Tyr
NM_001145280.3:c.-11+28551A>T	NP_001138752.1:n.-11+28551A>T
NM_001145281.2:c.47+29010A>T	NP_001138753.1:n.47+29010A>T
NM_001145282.2:c.25A>T	NP_001138754.1:p.Asn9Tyr
NM_001145283.2:c.25A>T	NP_001138755.1:p.Asn9Tyr
NM_001145284.3:c.25A>T	NP_001138756.1:p.Asn9Tyr
NM_001145285.2:c.25A>T	NP_001138757.1:p.Asn9Tyr
NM_001145286.2:c.25A>T	NP_001138758.1:p.Asn9Tyr
NM_001285522.1:c.25A>T	NP_001272451.1:p.Asn9Tyr
NM_001285523.1:c.25A>T	NP_001272452.1:p.Asn9Tyr
NM_001285524.1:c.304A>T	NP_001272453.1:p.Asn102Tyr
NR_104348.1:n.159A>T
NR_104349.1:n.159A>T
NR_104350.1:n.159A>T
NR_104351.1:n.159A>T
XM_006715497.2:c.211A>T	XP_006715560.1:p.Asn71Tyr
XM_011535849.1:c.304A>T	XP_011534151.1:p.Asn102Tyr
NM_001285523.2:c.25A>T	NP_001272452.1:p.Asn9Tyr
XM_017010907.2:c.211A>T	XP_016866396.1:p.Asn71Tyr
NM_000914.5:c.25A>T MANE Select	NP_000905.3:p.Asn9Tyr
NM_001008503.3:c.25A>T	NP_001008503.2:p.Asn9Tyr
NM_001008504.4:c.25A>T	NP_001008504.2:p.Asn9Tyr
NM_001145279.4:c.304A>T	NP_001138751.1:p.Asn102Tyr
NM_001145280.4:c.-11+28551A>T	NP_001138752.1:n.-11+28551A>T
NM_001145281.3:c.47+29010A>T	NP_001138753.1:n.47+29010A>T
NM_001145285.3:c.25A>T	NP_001138757.1:p.Asn9Tyr
NM_001145286.3:c.25A>T	NP_001138758.1:p.Asn9Tyr
NM_001285523.3:c.25A>T	NP_001272452.1:p.Asn9Tyr