Canonical Allele Identifier: CA2406578817

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127969A= , CM000684.2:g.42127969A=	GRCh38
NC_000022.10:g.42523971A= , CM000684.1:g.42523971A=	GRCh37
NC_000022.9:g.40853915A=	NCBI36
NG_008376.3:g.7023T=
NG_008376.4:g.7842T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.691-35T=	ENSP00000353241.6:n.691-35T=
ENST00000645361.2:c.858T= MANE Select	ENSP00000496150.1:p.Pro286=
ENST00000359033.4:c.705T=	ENSP00000351927.4:p.Pro235=
ENST00000360124.9:c.511-35T=	ENSP00000353241.5:n.511-35T=
ENST00000360608.9:c.858T=	ENSP00000353820.5:p.Pro286=
ENST00000389970.7:c.792T=	ENSP00000374620.4:p.Pro264=
ENST00000488442.1:n.1582T=
NM_000106.5:c.858T=	NP_000097.3:p.Pro286=
NM_001025161.2:c.705T=	NP_001020332.2:p.Pro235=
XM_011529966.1:c.858T=	XP_011528268.1:p.Pro286=
XM_011529967.1:c.858T=	XP_011528269.1:p.Pro286=
XM_011529968.1:c.858T=	XP_011528270.1:p.Pro286=
XM_011529969.1:c.714T=	XP_011528271.1:p.Pro238=
XM_011529970.1:c.705T=	XP_011528272.1:p.Pro235=
XM_011529971.1:c.714T=	XP_011528273.1:p.Pro238=
XM_011529972.1:c.843+205T=	XP_011528274.1:n.843+205T=
NM_000106.6:c.858T= MANE Select	NP_000097.3:p.Pro286=
NM_001025161.3:c.705T=	NP_001020332.2:p.Pro235=