Canonical Allele Identifier: CA2406578978

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128175T= , CM000684.2:g.42128175T=	GRCh38
NC_000022.10:g.42524177T= , CM000684.1:g.42524177T=	GRCh37
NC_000022.9:g.40854121T=	NCBI36
NG_008376.3:g.6817A=
NG_008376.4:g.7636A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.689A=	ENSP00000353241.6:p.Lys230=
ENST00000645361.2:c.842A= MANE Select	ENSP00000496150.1:p.Lys281=
ENST00000359033.4:c.689A=	ENSP00000351927.4:p.Lys230=
ENST00000360124.9:c.509A=	ENSP00000353241.5:p.Lys170=
ENST00000360608.9:c.842A=	ENSP00000353820.5:p.Lys281=
ENST00000389970.7:c.776A=	ENSP00000374620.4:p.Lys259=
ENST00000488442.1:n.1566A=
NM_000106.5:c.842A=	NP_000097.3:p.Lys281=
NM_001025161.2:c.689A=	NP_001020332.2:p.Lys230=
XM_011529966.1:c.842A=	XP_011528268.1:p.Lys281=
XM_011529967.1:c.842A=	XP_011528269.1:p.Lys281=
XM_011529968.1:c.842A=	XP_011528270.1:p.Lys281=
XM_011529969.1:c.698A=	XP_011528271.1:p.Lys233=
XM_011529970.1:c.689A=	XP_011528272.1:p.Lys230=
XM_011529971.1:c.698A=	XP_011528273.1:p.Lys233=
XM_011529972.1:c.842A=	XP_011528274.1:p.Lys281=
NM_000106.6:c.842A= MANE Select	NP_000097.3:p.Lys281=
NM_001025161.3:c.689A=	NP_001020332.2:p.Lys230=