Canonical Allele Identifier: CA4061686

Gene: OPRM1

Linked Data

• ClinVar Variation Id: 829156
• ClinVar RCV Id: RCV001029075
• dbSNP Id: rs562859
• ExAC: 6:154414573 C / T
• gnomAD v2: 6-154414573-C-T
• gnomAD v3: 6-154093438-C-T
• gnomAD v4: 6-154093438-C-T
• MyVariant Identifiers: chr6:g.154414573C>T (hg19) ; chr6:g.154093438C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154093438C>T , CM000668.2:g.154093438C>T	GRCh38
NC_000006.11:g.154414573C>T , CM000668.1:g.154414573C>T	GRCh37
NC_000006.10:g.154456266C>T	NCBI36
NG_021208.1:g.87938C>T
NG_021208.2:g.87938C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000330432.12:c.1164+1966C>T MANE Select	ENSP00000328264.7:n.1164+1966C>T
ENST00000229768.9:c.1333C>T	ENSP00000229768.5:p.Leu445=
ENST00000330432.11:c.1164+1966C>T	ENSP00000328264.7:n.1164+1966C>T
ENST00000337049.8:c.1164+1966C>T	ENSP00000338381.4:n.1164+1966C>T
ENST00000414028.6:c.1164+1966C>T	ENSP00000399359.2:n.1164+1966C>T
ENST00000419506.6:c.1164+1966C>T	ENSP00000403549.2:n.1164+1966C>T
ENST00000434900.6:c.1443+1966C>T	ENSP00000394624.2:n.1443+1966C>T
ENST00000435918.6:c.1164+1966C>T	ENSP00000413752.2:n.1164+1966C>T
ENST00000452687.6:c.1164+1966C>T	ENSP00000410497.2:n.1164+1966C>T
ENST00000518759.5:c.921+1966C>T	ENSP00000430260.1:n.921+1966C>T
ENST00000519083.5:c.1165-772C>T	ENSP00000431048.1:n.1165-772C>T
ENST00000519613.5:n.1096+1966C>T
ENST00000520708.5:c.864+1966C>T	ENSP00000430876.1:n.864+1966C>T
ENST00000522236.1:c.864+1966C>T	ENSP00000429373.1:n.864+1966C>T
ENST00000522555.5:c.864+1966C>T	ENSP00000429719.1:n.864+1966C>T
ENST00000522739.5:c.1165-772C>T	ENSP00000428018.1:n.1165-772C>T
ENST00000524150.2:c.*250+1966C>T	ENSP00000430575.1:n.*250+1966C>T
ENST00000524163.5:c.1164+1966C>T	ENSP00000430097.1:n.1164+1966C>T
NM_000914.4:c.1164+1966C>T	NP_000905.3:n.1164+1966C>T
NM_001008503.2:c.1164+1966C>T	NP_001008503.2:n.1164+1966C>T
NM_001008505.2:c.1333C>T	NP_001008505.2:p.Leu445=
NM_001145279.3:c.1443+1966C>T	NP_001138751.1:n.1443+1966C>T
NM_001145280.3:c.864+1966C>T	NP_001138752.1:n.864+1966C>T
NM_001145281.2:c.921+1966C>T	NP_001138753.1:n.921+1966C>T
NM_001145282.2:c.1164+1966C>T	NP_001138754.1:n.1164+1966C>T
NM_001145283.2:c.1164+1966C>T	NP_001138755.1:n.1164+1966C>T
NM_001145284.3:c.1164+1966C>T	NP_001138756.1:n.1164+1966C>T
NM_001145285.2:c.1164+1966C>T	NP_001138757.1:n.1164+1966C>T
NM_001145286.2:c.1164+1966C>T	NP_001138758.1:n.1164+1966C>T
NM_001145287.2:c.864+1966C>T	NP_001138759.1:n.864+1966C>T
NM_001285522.1:c.291-25245C>T	NP_001272451.1:n.291-25245C>T
NM_001285524.1:c.1443+1966C>T	NP_001272453.1:n.1443+1966C>T
NM_001285526.1:c.864+1966C>T	NP_001272455.1:n.864+1966C>T
NR_104348.1:n.1299-772C>T
NR_104349.1:n.1299-772C>T
NR_104350.1:n.945+1966C>T
NR_104351.1:n.1299-772C>T
XM_011535849.1:c.1443+1966C>T	XP_011534151.1:n.1443+1966C>T
XM_011535850.1:c.1126C>T	XP_011534152.1:p.Leu376=
XM_011535851.1:c.1033C>T	XP_011534153.1:p.Leu345=
XM_011535852.1:c.1033C>T	XP_011534154.1:p.Leu345=
XM_011535853.1:c.1033C>T	XP_011534155.1:p.Leu345=
XM_011535854.1:c.1033C>T	XP_011534156.1:p.Leu345=
XM_011535855.1:c.1033C>T	XP_011534157.1:p.Leu345=
XM_011535856.1:c.1033C>T	XP_011534158.1:p.Leu345=
XM_011535857.1:c.1033C>T	XP_011534159.1:p.Leu345=
XM_011535858.1:c.1033C>T	XP_011534160.1:p.Leu345=
XM_011535859.1:c.864+1966C>T	XP_011534161.1:n.864+1966C>T
XM_011535860.1:c.864+1966C>T	XP_011534162.1:n.864+1966C>T
XM_011535861.1:c.864+1966C>T	XP_011534163.1:n.864+1966C>T
XM_011535862.1:c.1033C>T	XP_011534164.1:p.Leu345=
XM_011535851.3:c.1033C>T	XP_011534153.1:p.Leu345=
XM_011535853.2:c.1033C>T	XP_011534155.1:p.Leu345=
XM_011535856.2:c.1033C>T	XP_011534158.1:p.Leu345=
XM_011535862.2:c.1033C>T	XP_011534164.1:p.Leu345=
XM_017010903.2:c.1033C>T	XP_016866392.1:p.Leu345=
XM_017010904.1:c.1033C>T	XP_016866393.1:p.Leu345=
XM_017010905.1:c.1033C>T	XP_016866394.1:p.Leu345=
XM_017010906.2:c.864+1966C>T	XP_016866395.1:n.864+1966C>T
NM_000914.5:c.1164+1966C>T MANE Select	NP_000905.3:n.1164+1966C>T
NM_001008503.3:c.1164+1966C>T	NP_001008503.2:n.1164+1966C>T
NM_001145279.4:c.1443+1966C>T	NP_001138751.1:n.1443+1966C>T
NM_001145280.4:c.864+1966C>T	NP_001138752.1:n.864+1966C>T
NM_001145281.3:c.921+1966C>T	NP_001138753.1:n.921+1966C>T
NM_001145285.3:c.1164+1966C>T	NP_001138757.1:n.1164+1966C>T
NM_001145286.3:c.1164+1966C>T	NP_001138758.1:n.1164+1966C>T
NM_001145287.3:c.864+1966C>T	NP_001138759.1:n.864+1966C>T
NM_001285526.2:c.864+1966C>T	NP_001272455.1:n.864+1966C>T