Canonical Allele Identifier: CA2406578762

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127895G= , CM000684.2:g.42127895G=	GRCh38
NC_000022.10:g.42523897G= , CM000684.1:g.42523897G=	GRCh37
NC_000022.9:g.40853841G=	NCBI36
NG_008376.3:g.7097C=
NG_008376.4:g.7916C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.932C= MANE Select	NP_000097.3:p.Ser311=
ENST00000645361.2:c.932C= MANE Select	ENSP00000496150.1:p.Ser311=
NM_000106.5:c.932C=	NP_000097.3:p.Ser311=
NM_001025161.2:c.779C=	NP_001020332.2:p.Ser260=
NM_001025161.3:c.779C=	NP_001020332.2:p.Ser260=
ENST00000359033.4:c.779C=	ENSP00000351927.4:p.Ser260=
ENST00000360124.10:c.730C=	ENSP00000353241.6:n.730C=
ENST00000360124.9:c.550C=	ENSP00000353241.5:n.550C=
ENST00000360608.9:c.932C=	ENSP00000353820.5:p.Ser311=
ENST00000389970.7:c.866C=	ENSP00000374620.4:p.Ser289=
ENST00000488442.1:n.1656C=
XM_011529966.1:c.932C=	XP_011528268.1:p.Ser311=
XM_011529967.1:c.932C=	XP_011528269.1:p.Ser311=
XM_011529968.1:c.932C=	XP_011528270.1:p.Ser311=
XM_011529969.1:c.788C=	XP_011528271.1:p.Ser263=
XM_011529970.1:c.779C=	XP_011528272.1:p.Ser260=
XM_011529971.1:c.788C=	XP_011528273.1:p.Ser263=
XM_011529972.1:c.844-261C=	XP_011528274.1:n.844-261C=