Canonical Allele Identifier: CA2406579776

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129171G= , CM000684.2:g.42129171G=	GRCh38
NC_000022.10:g.42525173G= , CM000684.1:g.42525173G=	GRCh37
NC_000022.9:g.40855117G=	NCBI36
NG_008376.3:g.5821C=
NG_008376.4:g.6640C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-227C=	ENSP00000353241.6:n.353-227C=
ENST00000645361.2:c.367C= MANE Select	ENSP00000496150.1:p.Arg123=
ENST00000359033.4:c.353-227C=	ENSP00000351927.4:n.353-227C=
ENST00000360124.9:c.173-227C=	ENSP00000353241.5:n.173-227C=
ENST00000360608.9:c.367C=	ENSP00000353820.5:p.Arg123=
ENST00000389970.7:c.301C=	ENSP00000374620.4:p.Arg101=
ENST00000488442.1:n.1091C=
NM_000106.5:c.367C=	NP_000097.3:p.Arg123=
NM_001025161.2:c.353-227C=	NP_001020332.2:n.353-227C=
XM_011529966.1:c.367C=	XP_011528268.1:p.Arg123=
XM_011529967.1:c.367C=	XP_011528269.1:p.Arg123=
XM_011529968.1:c.367C=	XP_011528270.1:p.Arg123=
XM_011529969.1:c.224C=	XP_011528271.1:p.Ala75=
XM_011529970.1:c.353-227C=	XP_011528272.1:n.353-227C=
XM_011529971.1:c.224C=	XP_011528273.1:p.Ala75=
XM_011529972.1:c.367C=	XP_011528274.1:p.Arg123=
NM_000106.6:c.367C= MANE Select	NP_000097.3:p.Arg123=
NM_001025161.3:c.353-227C=	NP_001020332.2:n.353-227C=