Canonical Allele Identifier: CA2406577822

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126627A= , CM000684.2:g.42126627A=	GRCh38
NC_000022.10:g.42522629A= , CM000684.1:g.42522629A=	GRCh37
NC_000022.9:g.40852573A=	NCBI36
NG_008376.3:g.8365T=
NG_008376.4:g.9184T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1239T=	ENSP00000353241.6:n.1239T=
ENST00000645361.2:c.1441T= MANE Select	ENSP00000496150.1:p.Phe481=
ENST00000359033.4:c.1288T=	ENSP00000351927.4:p.Phe430=
ENST00000360124.9:c.1059T=	ENSP00000353241.5:n.1059T=
ENST00000360608.9:c.1441T=	ENSP00000353820.5:p.Phe481=
ENST00000389970.7:c.1432T=	ENSP00000374620.4:p.Phe478=
ENST00000488442.1:n.2165T=
NM_000106.5:c.1441T=	NP_000097.3:p.Phe481=
NM_001025161.2:c.1288T=	NP_001020332.2:p.Phe430=
XM_011529966.1:c.1441T=	XP_011528268.1:p.Phe481=
XM_011529967.1:c.1441T=	XP_011528269.1:p.Phe481=
XM_011529968.1:c.1441T=	XP_011528270.1:p.Phe481=
XM_011529969.1:c.1297T=	XP_011528271.1:p.Phe433=
XM_011529970.1:c.1288T=	XP_011528272.1:p.Phe430=
XM_011529971.1:c.1297T=	XP_011528273.1:p.Phe433=
NM_000106.6:c.1441T= MANE Select	NP_000097.3:p.Phe481=
NM_001025161.3:c.1288T=	NP_001020332.2:p.Phe430=