Canonical Allele Identifier: CA2406579021

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128222G= , CM000684.2:g.42128222G=	GRCh38
NC_000022.10:g.42524224G= , CM000684.1:g.42524224G=	GRCh37
NC_000022.9:g.40854168G=	NCBI36
NG_008376.3:g.6770C=
NG_008376.4:g.7589C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.642C=	ENSP00000353241.6:p.Ala214=
ENST00000645361.2:c.795C= MANE Select	ENSP00000496150.1:p.Ala265=
ENST00000359033.4:c.642C=	ENSP00000351927.4:p.Ala214=
ENST00000360124.9:c.462C=	ENSP00000353241.5:p.Ala154=
ENST00000360608.9:c.795C=	ENSP00000353820.5:p.Ala265=
ENST00000389970.7:c.729C=	ENSP00000374620.4:p.Ala243=
ENST00000488442.1:n.1519C=
NM_000106.5:c.795C=	NP_000097.3:p.Ala265=
NM_001025161.2:c.642C=	NP_001020332.2:p.Ala214=
XM_011529966.1:c.795C=	XP_011528268.1:p.Ala265=
XM_011529967.1:c.795C=	XP_011528269.1:p.Ala265=
XM_011529968.1:c.795C=	XP_011528270.1:p.Ala265=
XM_011529969.1:c.651C=	XP_011528271.1:p.Ala217=
XM_011529970.1:c.642C=	XP_011528272.1:p.Ala214=
XM_011529971.1:c.651C=	XP_011528273.1:p.Ala217=
XM_011529972.1:c.795C=	XP_011528274.1:p.Ala265=
NM_000106.6:c.795C= MANE Select	NP_000097.3:p.Ala265=
NM_001025161.3:c.642C=	NP_001020332.2:p.Ala214=