Canonical Allele Identifier: CA2406580120

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129537G= , CM000684.2:g.42129537G=	GRCh38
NC_000022.10:g.42525539G= , CM000684.1:g.42525539G=	GRCh37
NC_000022.9:g.40855483G=	NCBI36
NG_008376.3:g.5455C=
NG_008376.4:g.6274C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.352+201C=	ENSP00000353241.6:n.352+201C=
ENST00000645361.2:c.352+201C= MANE Select	ENSP00000496150.1:n.352+201C=
ENST00000359033.4:c.352+201C=	ENSP00000351927.4:n.352+201C=
ENST00000360124.9:c.172+201C=	ENSP00000353241.5:n.172+201C=
ENST00000360608.9:c.352+201C=	ENSP00000353820.5:n.352+201C=
ENST00000389970.7:c.286+201C=	ENSP00000374620.4:n.286+201C=
ENST00000488442.1:n.1076+201C=
NM_000106.5:c.352+201C=	NP_000097.3:n.352+201C=
NM_001025161.2:c.352+201C=	NP_001020332.2:n.352+201C=
XM_011529966.1:c.352+201C=	XP_011528268.1:n.352+201C=
XM_011529967.1:c.352+201C=	XP_011528269.1:n.352+201C=
XM_011529968.1:c.352+201C=	XP_011528270.1:n.352+201C=
XM_011529969.1:c.209+201C=	XP_011528271.1:n.209+201C=
XM_011529970.1:c.352+201C=	XP_011528272.1:n.352+201C=
XM_011529971.1:c.209+201C=	XP_011528273.1:n.209+201C=
XM_011529972.1:c.352+201C=	XP_011528274.1:n.352+201C=
NM_000106.6:c.352+201C= MANE Select	NP_000097.3:n.352+201C=
NM_001025161.3:c.352+201C=	NP_001020332.2:n.352+201C=