Canonical Allele Identifier: CA2406579681

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129043G= , CM000684.2:g.42129043G=	GRCh38
NC_000022.10:g.42525045G= , CM000684.1:g.42525045G=	GRCh37
NC_000022.9:g.40854989G=	NCBI36
NG_008376.3:g.5949C=
NG_008376.4:g.6768C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-99C=	ENSP00000353241.6:n.353-99C=
ENST00000645361.2:c.495C= MANE Select	ENSP00000496150.1:p.Ala165=
ENST00000359033.4:c.353-99C=	ENSP00000351927.4:n.353-99C=
ENST00000360124.9:c.173-99C=	ENSP00000353241.5:n.173-99C=
ENST00000360608.9:c.495C=	ENSP00000353820.5:p.Ala165=
ENST00000389970.7:c.429C=	ENSP00000374620.4:p.Ala143=
ENST00000488442.1:n.1219C=
NM_000106.5:c.495C=	NP_000097.3:p.Ala165=
NM_001025161.2:c.353-99C=	NP_001020332.2:n.353-99C=
XM_011529966.1:c.495C=	XP_011528268.1:p.Ala165=
XM_011529967.1:c.495C=	XP_011528269.1:p.Ala165=
XM_011529968.1:c.495C=	XP_011528270.1:p.Ala165=
XM_011529969.1:c.352C=	XP_011528271.1:p.Gln118=
XM_011529970.1:c.353-99C=	XP_011528272.1:n.353-99C=
XM_011529971.1:c.352C=	XP_011528273.1:p.Gln118=
XM_011529972.1:c.495C=	XP_011528274.1:p.Ala165=
NM_000106.6:c.495C= MANE Select	NP_000097.3:p.Ala165=
NM_001025161.3:c.353-99C=	NP_001020332.2:n.353-99C=