Canonical Allele Identifier: CA2406579780

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42129175C= , CM000684.2:g.42129175C=	GRCh38
NC_000022.10:g.42525177C= , CM000684.1:g.42525177C=	GRCh37
NC_000022.9:g.40855121C=	NCBI36
NG_008376.3:g.5817G=
NG_008376.4:g.6636G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.353-231G=	ENSP00000353241.6:n.353-231G=
ENST00000645361.2:c.363G= MANE Select	ENSP00000496150.1:p.Leu121=
ENST00000359033.4:c.353-231G=	ENSP00000351927.4:n.353-231G=
ENST00000360124.9:c.173-231G=	ENSP00000353241.5:n.173-231G=
ENST00000360608.9:c.363G=	ENSP00000353820.5:p.Leu121=
ENST00000389970.7:c.297G=	ENSP00000374620.4:p.Leu99=
ENST00000488442.1:n.1087G=
NM_000106.5:c.363G=	NP_000097.3:p.Leu121=
NM_001025161.2:c.353-231G=	NP_001020332.2:n.353-231G=
XM_011529966.1:c.363G=	XP_011528268.1:p.Leu121=
XM_011529967.1:c.363G=	XP_011528269.1:p.Leu121=
XM_011529968.1:c.363G=	XP_011528270.1:p.Leu121=
XM_011529969.1:c.220G=	XP_011528271.1:p.Gly74=
XM_011529970.1:c.353-231G=	XP_011528272.1:n.353-231G=
XM_011529971.1:c.220G=	XP_011528273.1:p.Gly74=
XM_011529972.1:c.363G=	XP_011528274.1:p.Leu121=
NM_000106.6:c.363G= MANE Select	NP_000097.3:p.Leu121=
NM_001025161.3:c.353-231G=	NP_001020332.2:n.353-231G=