Canonical Allele Identifier: CA2406580211

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129637T= , CM000684.2:g.42129637T=	GRCh38
NC_000022.10:g.42525639T= , CM000684.1:g.42525639T=	GRCh37
NC_000022.9:g.40855583T=	NCBI36
NG_008376.3:g.5355A=
NG_008376.4:g.6174A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.352+101A=	ENSP00000353241.6:n.352+101A=
ENST00000645361.2:c.352+101A= MANE Select	ENSP00000496150.1:n.352+101A=
ENST00000359033.4:c.352+101A=	ENSP00000351927.4:n.352+101A=
ENST00000360124.9:c.172+101A=	ENSP00000353241.5:n.172+101A=
ENST00000360608.9:c.352+101A=	ENSP00000353820.5:n.352+101A=
ENST00000389970.7:c.286+101A=	ENSP00000374620.4:n.286+101A=
ENST00000488442.1:n.1076+101A=
NM_000106.5:c.352+101A=	NP_000097.3:n.352+101A=
NM_001025161.2:c.352+101A=	NP_001020332.2:n.352+101A=
XM_011529966.1:c.352+101A=	XP_011528268.1:n.352+101A=
XM_011529967.1:c.352+101A=	XP_011528269.1:n.352+101A=
XM_011529968.1:c.352+101A=	XP_011528270.1:n.352+101A=
XM_011529969.1:c.209+101A=	XP_011528271.1:n.209+101A=
XM_011529970.1:c.352+101A=	XP_011528272.1:n.352+101A=
XM_011529971.1:c.209+101A=	XP_011528273.1:n.209+101A=
XM_011529972.1:c.352+101A=	XP_011528274.1:n.352+101A=
NM_000106.6:c.352+101A= MANE Select	NP_000097.3:n.352+101A=
NM_001025161.3:c.352+101A=	NP_001020332.2:n.352+101A=