Canonical Allele Identifier: CA2406579009

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128211C= , CM000684.2:g.42128211C=	GRCh38
NC_000022.10:g.42524213C= , CM000684.1:g.42524213C=	GRCh37
NC_000022.9:g.40854157C=	NCBI36
NG_008376.3:g.6781G=
NG_008376.4:g.7600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.653G=	ENSP00000353241.6:p.Arg218=
ENST00000645361.2:c.806G= MANE Select	ENSP00000496150.1:p.Arg269=
ENST00000359033.4:c.653G=	ENSP00000351927.4:p.Arg218=
ENST00000360124.9:c.473G=	ENSP00000353241.5:p.Arg158=
ENST00000360608.9:c.806G=	ENSP00000353820.5:p.Arg269=
ENST00000389970.7:c.740G=	ENSP00000374620.4:p.Arg247=
ENST00000488442.1:n.1530G=
NM_000106.5:c.806G=	NP_000097.3:p.Arg269=
NM_001025161.2:c.653G=	NP_001020332.2:p.Arg218=
XM_011529966.1:c.806G=	XP_011528268.1:p.Arg269=
XM_011529967.1:c.806G=	XP_011528269.1:p.Arg269=
XM_011529968.1:c.806G=	XP_011528270.1:p.Arg269=
XM_011529969.1:c.662G=	XP_011528271.1:p.Arg221=
XM_011529970.1:c.653G=	XP_011528272.1:p.Arg218=
XM_011529971.1:c.662G=	XP_011528273.1:p.Arg221=
XM_011529972.1:c.806G=	XP_011528274.1:p.Arg269=
NM_000106.6:c.806G= MANE Select	NP_000097.3:p.Arg269=
NM_001025161.3:c.653G=	NP_001020332.2:p.Arg218=