Canonical Allele Identifier: CA2406579478

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128801A= , CM000684.2:g.42128801A=	GRCh38
NC_000022.10:g.42524803A= , CM000684.1:g.42524803A=	GRCh37
NC_000022.9:g.40854747A=	NCBI36
NG_008376.3:g.6191T=
NG_008376.4:g.7010T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.496T=	ENSP00000353241.6:p.Ser166=
ENST00000645361.2:c.649T= MANE Select	ENSP00000496150.1:p.Ser217=
ENST00000359033.4:c.496T=	ENSP00000351927.4:p.Ser166=
ENST00000360124.9:c.316T=	ENSP00000353241.5:p.Ser106=
ENST00000360608.9:c.649T=	ENSP00000353820.5:p.Ser217=
ENST00000389970.7:c.583T=	ENSP00000374620.4:p.Ser195=
ENST00000488442.1:n.1373T=
NM_000106.5:c.649T=	NP_000097.3:p.Ser217=
NM_001025161.2:c.496T=	NP_001020332.2:p.Ser166=
XM_011529966.1:c.649T=	XP_011528268.1:p.Ser217=
XM_011529967.1:c.649T=	XP_011528269.1:p.Ser217=
XM_011529968.1:c.649T=	XP_011528270.1:p.Ser217=
XM_011529969.1:c.505T=	XP_011528271.1:p.Ser169=
XM_011529970.1:c.496T=	XP_011528272.1:p.Ser166=
XM_011529971.1:c.505T=	XP_011528273.1:p.Ser169=
XM_011529972.1:c.649T=	XP_011528274.1:p.Ser217=
NM_000106.6:c.649T= MANE Select	NP_000097.3:p.Ser217=
NM_001025161.3:c.496T=	NP_001020332.2:p.Ser166=