Canonical Allele Identifier: CA150238430

Gene: OPRM1

Linked Data

• dbSNP Id: rs906320525
• MyVariant Identifiers: chr6:g.154360563del (hg19) ; chr6:g.154039428del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154039429del , CM000668.2:g.154039429del	GRCh38
NC_000006.11:g.154360564del , CM000668.1:g.154360564del	GRCh37
NC_000006.10:g.154402257del	NCBI36
NG_021208.1:g.33929del
NG_021208.2:g.33929del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330432.12:c.-116del MANE Select	ENSP00000328264.7:n.-116del
ENST00000330432.11:c.-116del	ENSP00000328264.7:n.-116del
ENST00000360422.8:c.71del	ENSP00000353598.5:p.Lys24ArgfsTer?
ENST00000428397.6:c.-116del	ENSP00000411903.2:n.-116del
ENST00000434900.6:c.164del	ENSP00000394624.2:p.Lys55ArgfsTer?
ENST00000518759.5:c.47+28870del	ENSP00000430260.1:n.47+28870del
ENST00000520282.5:c.29del	ENSP00000430247.1:p.Lys10ArgfsTer?
ENST00000520708.5:c.-11+28411del	ENSP00000430876.1:n.-11+28411del
ENST00000523520.1:n.66del
NM_000914.4:c.-116del	NP_000905.3:n.-116del
NM_001008503.2:c.-116del	NP_001008503.2:n.-116del
NM_001008504.3:c.-116del	NP_001008504.2:n.-116del
NM_001008505.2:c.-116del	NP_001008505.2:n.-116del
NM_001145279.3:c.164del	NP_001138751.1:p.Lys55ArgfsTer?
NM_001145280.3:c.-11+28411del	NP_001138752.1:n.-11+28411del
NM_001145281.2:c.47+28870del	NP_001138753.1:n.47+28870del
NM_001145282.2:c.-116del	NP_001138754.1:n.-116del
NM_001145283.2:c.-116del	NP_001138755.1:n.-116del
NM_001145284.3:c.-116del	NP_001138756.1:n.-116del
NM_001145285.2:c.-116del	NP_001138757.1:n.-116del
NM_001145286.2:c.-116del	NP_001138758.1:n.-116del
NM_001285522.1:c.-116del	NP_001272451.1:n.-116del
NM_001285523.1:c.-116del	NP_001272452.1:n.-116del
NM_001285524.1:c.164del	NP_001272453.1:p.Lys55ArgfsTer?
NR_104348.1:n.19del
NR_104349.1:n.19del
NR_104350.1:n.19del
NR_104351.1:n.19del
XM_006715497.2:c.71del	XP_006715560.1:p.Lys24ArgfsTer?
XM_011535849.1:c.164del	XP_011534151.1:p.Lys55ArgfsTer?
NM_001285523.2:c.-116del	NP_001272452.1:n.-116del
XM_017010907.2:c.71del	XP_016866396.1:p.Lys24ArgfsTer?
NM_000914.5:c.-116del MANE Select	NP_000905.3:n.-116del
NM_001008503.3:c.-116del	NP_001008503.2:n.-116del
NM_001008504.4:c.-116del	NP_001008504.2:n.-116del
NM_001145279.4:c.164del	NP_001138751.1:p.Lys55ArgfsTer?
NM_001145280.4:c.-11+28411del	NP_001138752.1:n.-11+28411del
NM_001145281.3:c.47+28870del	NP_001138753.1:n.47+28870del
NM_001145285.3:c.-116del	NP_001138757.1:n.-116del
NM_001145286.3:c.-116del	NP_001138758.1:n.-116del
NM_001285523.3:c.-116del	NP_001272452.1:n.-116del