Canonical Allele Identifier: CA2406578470

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127500C= , CM000684.2:g.42127500C=	GRCh38
NC_000022.10:g.42523502C= , CM000684.1:g.42523502C=	GRCh37
NC_000022.9:g.40853446C=	NCBI36
NG_008376.3:g.7492G=
NG_008376.4:g.8311G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000106.6:c.1120G= MANE Select	NP_000097.3:p.Val374=
ENST00000645361.2:c.1120G= MANE Select	ENSP00000496150.1:p.Val374=
NM_000106.5:c.1120G=	NP_000097.3:p.Val374=
NM_001025161.2:c.967G=	NP_001020332.2:p.Val323=
NM_001025161.3:c.967G=	NP_001020332.2:p.Val323=
ENST00000359033.4:c.967G=	ENSP00000351927.4:p.Val323=
ENST00000360124.10:c.918G=	ENSP00000353241.6:n.918G=
ENST00000360124.9:c.738G=	ENSP00000353241.5:n.738G=
ENST00000360608.9:c.1120G=	ENSP00000353820.5:p.Val374=
ENST00000389970.7:c.1111G=	ENSP00000374620.4:p.Val371=
ENST00000488442.1:n.1844G=
XM_011529966.1:c.1120G=	XP_011528268.1:p.Val374=
XM_011529967.1:c.1120G=	XP_011528269.1:p.Val374=
XM_011529968.1:c.1120G=	XP_011528270.1:p.Val374=
XM_011529969.1:c.976G=	XP_011528271.1:p.Val326=
XM_011529970.1:c.967G=	XP_011528272.1:p.Val323=
XM_011529971.1:c.976G=	XP_011528273.1:p.Val326=