Canonical Allele Identifier: CA2406579553

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128891C= , CM000684.2:g.42128891C=	GRCh38
NC_000022.10:g.42524893C= , CM000684.1:g.42524893C=	GRCh37
NC_000022.9:g.40854837C=	NCBI36
NG_008376.3:g.6101G=
NG_008376.4:g.6920G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.406G=	ENSP00000353241.6:p.Ala136=
ENST00000645361.2:c.559G= MANE Select	ENSP00000496150.1:p.Ala187=
ENST00000359033.4:c.406G=	ENSP00000351927.4:p.Ala136=
ENST00000360124.9:c.226G=	ENSP00000353241.5:p.Ala76=
ENST00000360608.9:c.559G=	ENSP00000353820.5:p.Ala187=
ENST00000389970.7:c.493G=	ENSP00000374620.4:p.Ala165=
ENST00000488442.1:n.1283G=
NM_000106.5:c.559G=	NP_000097.3:p.Ala187=
NM_001025161.2:c.406G=	NP_001020332.2:p.Ala136=
XM_011529966.1:c.559G=	XP_011528268.1:p.Ala187=
XM_011529967.1:c.559G=	XP_011528269.1:p.Ala187=
XM_011529968.1:c.559G=	XP_011528270.1:p.Ala187=
XM_011529969.1:c.415G=	XP_011528271.1:p.Ala139=
XM_011529970.1:c.406G=	XP_011528272.1:p.Ala136=
XM_011529971.1:c.415G=	XP_011528273.1:p.Ala139=
XM_011529972.1:c.559G=	XP_011528274.1:p.Ala187=
NM_000106.6:c.559G= MANE Select	NP_000097.3:p.Ala187=
NM_001025161.3:c.406G=	NP_001020332.2:p.Ala136=