Canonical Allele Identifier: CA2406579470

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128793A= , CM000684.2:g.42128793A=	GRCh38
NC_000022.10:g.42524795A= , CM000684.1:g.42524795A=	GRCh37
NC_000022.9:g.40854739A=	NCBI36
NG_008376.3:g.6199T=
NG_008376.4:g.7018T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.504T=	ENSP00000353241.6:p.Phe168=
ENST00000645361.2:c.657T= MANE Select	ENSP00000496150.1:p.Phe219=
ENST00000359033.4:c.504T=	ENSP00000351927.4:p.Phe168=
ENST00000360124.9:c.324T=	ENSP00000353241.5:p.Phe108=
ENST00000360608.9:c.657T=	ENSP00000353820.5:p.Phe219=
ENST00000389970.7:c.591T=	ENSP00000374620.4:p.Phe197=
ENST00000488442.1:n.1381T=
NM_000106.5:c.657T=	NP_000097.3:p.Phe219=
NM_001025161.2:c.504T=	NP_001020332.2:p.Phe168=
XM_011529966.1:c.657T=	XP_011528268.1:p.Phe219=
XM_011529967.1:c.657T=	XP_011528269.1:p.Phe219=
XM_011529968.1:c.657T=	XP_011528270.1:p.Phe219=
XM_011529969.1:c.513T=	XP_011528271.1:p.Phe171=
XM_011529970.1:c.504T=	XP_011528272.1:p.Phe168=
XM_011529971.1:c.513T=	XP_011528273.1:p.Phe171=
XM_011529972.1:c.657T=	XP_011528274.1:p.Phe219=
NM_000106.6:c.657T= MANE Select	NP_000097.3:p.Phe219=
NM_001025161.3:c.504T=	NP_001020332.2:p.Phe168=