Canonical Allele Identifier: CA2406580322

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129757A= , CM000684.2:g.42129757A=	GRCh38
NC_000022.10:g.42525759A= , CM000684.1:g.42525759A=	GRCh37
NC_000022.9:g.40855703A=	NCBI36
NG_008376.3:g.5235T=
NG_008376.4:g.6054T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.333T= MANE Select	NP_000097.3:p.Gly111=
ENST00000645361.2:c.333T= MANE Select	ENSP00000496150.1:p.Gly111=
NM_000106.5:c.333T=	NP_000097.3:p.Gly111=
NM_001025161.2:c.333T=	NP_001020332.2:p.Gly111=
NM_001025161.3:c.333T=	NP_001020332.2:p.Gly111=
ENST00000359033.4:c.333T=	ENSP00000351927.4:p.Gly111=
ENST00000360124.10:c.333T=	ENSP00000353241.6:p.Gly111=
ENST00000360124.9:c.153T=	ENSP00000353241.5:p.Gly51=
ENST00000360608.9:c.333T=	ENSP00000353820.5:p.Gly111=
ENST00000389970.7:c.267T=	ENSP00000374620.4:p.Gly89=
ENST00000488442.1:n.1057T=
XM_011529966.1:c.333T=	XP_011528268.1:p.Gly111=
XM_011529967.1:c.333T=	XP_011528269.1:p.Gly111=
XM_011529968.1:c.333T=	XP_011528270.1:p.Gly111=
XM_011529969.1:c.190T=	XP_011528271.1:p.Phe64=
XM_011529970.1:c.333T=	XP_011528272.1:p.Gly111=
XM_011529971.1:c.190T=	XP_011528273.1:p.Phe64=
XM_011529972.1:c.333T=	XP_011528274.1:p.Gly111=