Canonical Allele Identifier: CA2406579814

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129211G= , CM000684.2:g.42129211G=	GRCh38
NC_000022.10:g.42525213G= , CM000684.1:g.42525213G=	GRCh37
NC_000022.9:g.40855157G=	NCBI36
NG_008376.3:g.5781C=
NG_008376.4:g.6600C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-267C=	ENSP00000353241.6:n.353-267C=
ENST00000645361.2:c.353-26C= MANE Select	ENSP00000496150.1:n.353-26C=
ENST00000359033.4:c.353-267C=	ENSP00000351927.4:n.353-267C=
ENST00000360124.9:c.173-267C=	ENSP00000353241.5:n.173-267C=
ENST00000360608.9:c.353-26C=	ENSP00000353820.5:n.353-26C=
ENST00000389970.7:c.287-26C=	ENSP00000374620.4:n.287-26C=
ENST00000488442.1:n.1077-26C=
NM_000106.5:c.353-26C=	NP_000097.3:n.353-26C=
NM_001025161.2:c.353-267C=	NP_001020332.2:n.353-267C=
XM_011529966.1:c.353-26C=	XP_011528268.1:n.353-26C=
XM_011529967.1:c.353-26C=	XP_011528269.1:n.353-26C=
XM_011529968.1:c.353-26C=	XP_011528270.1:n.353-26C=
XM_011529969.1:c.210-26C=	XP_011528271.1:n.210-26C=
XM_011529970.1:c.353-267C=	XP_011528272.1:n.353-267C=
XM_011529971.1:c.210-26C=	XP_011528273.1:n.210-26C=
XM_011529972.1:c.353-26C=	XP_011528274.1:n.353-26C=
NM_000106.6:c.353-26C= MANE Select	NP_000097.3:n.353-26C=
NM_001025161.3:c.353-267C=	NP_001020332.2:n.353-267C=