Canonical Allele Identifier: CA2406579570

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128914T= , CM000684.2:g.42128914T=	GRCh38
NC_000022.10:g.42524916T= , CM000684.1:g.42524916T=	GRCh37
NC_000022.9:g.40854860T=	NCBI36
NG_008376.3:g.6078A=
NG_008376.4:g.6897A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.383A=	ENSP00000353241.6:p.Asp128=
ENST00000645361.2:c.536A= MANE Select	ENSP00000496150.1:p.Asp179=
ENST00000359033.4:c.383A=	ENSP00000351927.4:p.Asp128=
ENST00000360124.9:c.203A=	ENSP00000353241.5:p.Asp68=
ENST00000360608.9:c.536A=	ENSP00000353820.5:p.Asp179=
ENST00000389970.7:c.470A=	ENSP00000374620.4:p.Asp157=
ENST00000488442.1:n.1260A=
NM_000106.5:c.536A=	NP_000097.3:p.Asp179=
NM_001025161.2:c.383A=	NP_001020332.2:p.Asp128=
XM_011529966.1:c.536A=	XP_011528268.1:p.Asp179=
XM_011529967.1:c.536A=	XP_011528269.1:p.Asp179=
XM_011529968.1:c.536A=	XP_011528270.1:p.Asp179=
XM_011529969.1:c.392A=	XP_011528271.1:p.Asp131=
XM_011529970.1:c.383A=	XP_011528272.1:p.Asp128=
XM_011529971.1:c.392A=	XP_011528273.1:p.Asp131=
XM_011529972.1:c.536A=	XP_011528274.1:p.Asp179=
NM_000106.6:c.536A= MANE Select	NP_000097.3:p.Asp179=
NM_001025161.3:c.383A=	NP_001020332.2:p.Asp128=