Canonical Allele Identifier: CA2406578445

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127457C= , CM000684.2:g.42127457C=	GRCh38
NC_000022.10:g.42523459C= , CM000684.1:g.42523459C=	GRCh37
NC_000022.9:g.40853403C=	NCBI36
NG_008376.3:g.7535G=
NG_008376.4:g.8354G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1163G= MANE Select	NP_000097.3:p.Arg388=
ENST00000645361.2:c.1163G= MANE Select	ENSP00000496150.1:p.Arg388=
NM_000106.5:c.1163G=	NP_000097.3:p.Arg388=
NM_001025161.2:c.1010G=	NP_001020332.2:p.Arg337=
NM_001025161.3:c.1010G=	NP_001020332.2:p.Arg337=
ENST00000359033.4:c.1010G=	ENSP00000351927.4:p.Arg337=
ENST00000360124.10:c.961G=	ENSP00000353241.6:n.961G=
ENST00000360124.9:c.781G=	ENSP00000353241.5:n.781G=
ENST00000360608.9:c.1163G=	ENSP00000353820.5:p.Arg388=
ENST00000389970.7:c.1154G=	ENSP00000374620.4:p.Arg385=
ENST00000488442.1:n.1887G=
XM_011529966.1:c.1163G=	XP_011528268.1:p.Arg388=
XM_011529967.1:c.1163G=	XP_011528269.1:p.Arg388=
XM_011529968.1:c.1163G=	XP_011528270.1:p.Arg388=
XM_011529969.1:c.1019G=	XP_011528271.1:p.Arg340=
XM_011529970.1:c.1010G=	XP_011528272.1:p.Arg337=
XM_011529971.1:c.1019G=	XP_011528273.1:p.Arg340=