Canonical Allele Identifier: CA2406578521

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127565T= , CM000684.2:g.42127565T=	GRCh38
NC_000022.10:g.42523567T= , CM000684.1:g.42523567T=	GRCh37
NC_000022.9:g.40853511T=	NCBI36
NG_008376.3:g.7427A=
NG_008376.4:g.8246A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1055A= MANE Select	NP_000097.3:p.His352=
ENST00000645361.2:c.1055A= MANE Select	ENSP00000496150.1:p.His352=
NM_000106.5:c.1055A=	NP_000097.3:p.His352=
NM_001025161.2:c.902A=	NP_001020332.2:p.His301=
NM_001025161.3:c.902A=	NP_001020332.2:p.His301=
ENST00000359033.4:c.902A=	ENSP00000351927.4:p.His301=
ENST00000360124.10:c.853A=	ENSP00000353241.6:n.853A=
ENST00000360124.9:c.673A=	ENSP00000353241.5:n.673A=
ENST00000360608.9:c.1055A=	ENSP00000353820.5:p.His352=
ENST00000389970.7:c.1046A=	ENSP00000374620.4:p.His349=
ENST00000488442.1:n.1779A=
XM_011529966.1:c.1055A=	XP_011528268.1:p.His352=
XM_011529967.1:c.1055A=	XP_011528269.1:p.His352=
XM_011529968.1:c.1055A=	XP_011528270.1:p.His352=
XM_011529969.1:c.911A=	XP_011528271.1:p.His304=
XM_011529970.1:c.902A=	XP_011528272.1:p.His301=
XM_011529971.1:c.911A=	XP_011528273.1:p.His304=
XM_011529972.1:c.*40A=	XP_011528274.1:n.*40A=