Canonical Allele Identifier: CA2406579007

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128210T= , CM000684.2:g.42128210T=	GRCh38
NC_000022.10:g.42524212T= , CM000684.1:g.42524212T=	GRCh37
NC_000022.9:g.40854156T=	NCBI36
NG_008376.3:g.6782A=
NG_008376.4:g.7601A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.654A=	ENSP00000353241.6:p.Arg218=
ENST00000645361.2:c.807A= MANE Select	ENSP00000496150.1:p.Arg269=
ENST00000359033.4:c.654A=	ENSP00000351927.4:p.Arg218=
ENST00000360124.9:c.474A=	ENSP00000353241.5:p.Arg158=
ENST00000360608.9:c.807A=	ENSP00000353820.5:p.Arg269=
ENST00000389970.7:c.741A=	ENSP00000374620.4:p.Arg247=
ENST00000488442.1:n.1531A=
NM_000106.5:c.807A=	NP_000097.3:p.Arg269=
NM_001025161.2:c.654A=	NP_001020332.2:p.Arg218=
XM_011529966.1:c.807A=	XP_011528268.1:p.Arg269=
XM_011529967.1:c.807A=	XP_011528269.1:p.Arg269=
XM_011529968.1:c.807A=	XP_011528270.1:p.Arg269=
XM_011529969.1:c.663A=	XP_011528271.1:p.Arg221=
XM_011529970.1:c.654A=	XP_011528272.1:p.Arg218=
XM_011529971.1:c.663A=	XP_011528273.1:p.Arg221=
XM_011529972.1:c.807A=	XP_011528274.1:p.Arg269=
NM_000106.6:c.807A= MANE Select	NP_000097.3:p.Arg269=
NM_001025161.3:c.654A=	NP_001020332.2:p.Arg218=