Canonical Allele Identifier: CA2406578753

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42127884C= , CM000684.2:g.42127884C=	GRCh38
NC_000022.10:g.42523886C= , CM000684.1:g.42523886C=	GRCh37
NC_000022.9:g.40853830C=	NCBI36
NG_008376.3:g.7108G=
NG_008376.4:g.7927G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.741G=	ENSP00000353241.6:n.741G=
ENST00000645361.2:c.943G= MANE Select	ENSP00000496150.1:p.Ala315=
ENST00000359033.4:c.790G=	ENSP00000351927.4:p.Ala264=
ENST00000360124.9:c.561G=	ENSP00000353241.5:n.561G=
ENST00000360608.9:c.943G=	ENSP00000353820.5:p.Ala315=
ENST00000389970.7:c.877G=	ENSP00000374620.4:p.Ala293=
ENST00000488442.1:n.1667G=
NM_000106.5:c.943G=	NP_000097.3:p.Ala315=
NM_001025161.2:c.790G=	NP_001020332.2:p.Ala264=
XM_011529966.1:c.943G=	XP_011528268.1:p.Ala315=
XM_011529967.1:c.943G=	XP_011528269.1:p.Ala315=
XM_011529968.1:c.943G=	XP_011528270.1:p.Ala315=
XM_011529969.1:c.799G=	XP_011528271.1:p.Ala267=
XM_011529970.1:c.790G=	XP_011528272.1:p.Ala264=
XM_011529971.1:c.799G=	XP_011528273.1:p.Ala267=
XM_011529972.1:c.844-250G=	XP_011528274.1:n.844-250G=
NM_000106.6:c.943G= MANE Select	NP_000097.3:p.Ala315=
NM_001025161.3:c.790G=	NP_001020332.2:p.Ala264=