Canonical Allele Identifier: CA2406578469

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127499A= , CM000684.2:g.42127499A=	GRCh38
NC_000022.10:g.42523501A= , CM000684.1:g.42523501A=	GRCh37
NC_000022.9:g.40853445A=	NCBI36
NG_008376.3:g.7493T=
NG_008376.4:g.8312T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.919T=	ENSP00000353241.6:n.919T=
ENST00000645361.2:c.1121T= MANE Select	ENSP00000496150.1:p.Val374=
ENST00000359033.4:c.968T=	ENSP00000351927.4:p.Val323=
ENST00000360124.9:c.739T=	ENSP00000353241.5:n.739T=
ENST00000360608.9:c.1121T=	ENSP00000353820.5:p.Val374=
ENST00000389970.7:c.1112T=	ENSP00000374620.4:p.Val371=
ENST00000488442.1:n.1845T=
NM_000106.5:c.1121T=	NP_000097.3:p.Val374=
NM_001025161.2:c.968T=	NP_001020332.2:p.Val323=
XM_011529966.1:c.1121T=	XP_011528268.1:p.Val374=
XM_011529967.1:c.1121T=	XP_011528269.1:p.Val374=
XM_011529968.1:c.1121T=	XP_011528270.1:p.Val374=
XM_011529969.1:c.977T=	XP_011528271.1:p.Val326=
XM_011529970.1:c.968T=	XP_011528272.1:p.Val323=
XM_011529971.1:c.977T=	XP_011528273.1:p.Val326=
NM_000106.6:c.1121T= MANE Select	NP_000097.3:p.Val374=
NM_001025161.3:c.968T=	NP_001020332.2:p.Val323=