Canonical Allele Identifier: CA2406577880

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126722G= , CM000684.2:g.42126722G=	GRCh38
NC_000022.10:g.42522724G= , CM000684.1:g.42522724G=	GRCh37
NC_000022.9:g.40852668G=	NCBI36
NG_008376.3:g.8270C=
NG_008376.4:g.9089C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1346C= MANE Select	NP_000097.3:p.Ala449=
ENST00000645361.2:c.1346C= MANE Select	ENSP00000496150.1:p.Ala449=
NM_000106.5:c.1346C=	NP_000097.3:p.Ala449=
NM_001025161.2:c.1193C=	NP_001020332.2:p.Ala398=
NM_001025161.3:c.1193C=	NP_001020332.2:p.Ala398=
ENST00000359033.4:c.1193C=	ENSP00000351927.4:p.Ala398=
ENST00000360124.10:c.1144C=	ENSP00000353241.6:n.1144C=
ENST00000360124.9:c.964C=	ENSP00000353241.5:n.964C=
ENST00000360608.9:c.1346C=	ENSP00000353820.5:p.Ala449=
ENST00000389970.7:c.1337C=	ENSP00000374620.4:p.Ala446=
ENST00000488442.1:n.2070C=
XM_011529966.1:c.1346C=	XP_011528268.1:p.Ala449=
XM_011529967.1:c.1346C=	XP_011528269.1:p.Ala449=
XM_011529968.1:c.1346C=	XP_011528270.1:p.Ala449=
XM_011529969.1:c.1202C=	XP_011528271.1:p.Ala401=
XM_011529970.1:c.1193C=	XP_011528272.1:p.Ala398=
XM_011529971.1:c.1202C=	XP_011528273.1:p.Ala401=