Canonical Allele Identifier: CA2406577765

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126536T= , CM000684.2:g.42126536T=	GRCh38
NC_000022.10:g.42522538T= , CM000684.1:g.42522538T=	GRCh37
NC_000022.9:g.40852482T=	NCBI36
NG_008376.3:g.8456A=
NG_008376.4:g.9275A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1330A=	ENSP00000353241.6:n.1330A=
ENST00000645361.2:c.*38A= MANE Select	ENSP00000496150.1:n.*38A=
ENST00000360124.9:c.1150A=	ENSP00000353241.5:n.1150A=
ENST00000360608.9:c.*38A=	ENSP00000353820.5:n.*38A=
ENST00000389970.7:c.*38A=	ENSP00000374620.4:n.*38A=
ENST00000488442.1:n.2256A=
NM_000106.5:c.*38A=	NP_000097.3:n.*38A=
NM_001025161.2:c.*38A=	NP_001020332.2:n.*38A=
XM_011529966.1:c.1452+80A=	XP_011528268.1:n.1452+80A=
XM_011529967.1:c.1452+80A=	XP_011528269.1:n.1452+80A=
XM_011529968.1:c.1452+80A=	XP_011528270.1:n.1452+80A=
XM_011529969.1:c.1308+80A=	XP_011528271.1:n.1308+80A=
XM_011529970.1:c.1299+80A=	XP_011528272.1:n.1299+80A=
XM_011529971.1:c.*38A=	XP_011528273.1:n.*38A=
NM_000106.6:c.*38A= MANE Select	NP_000097.3:n.*38A=
NM_001025161.3:c.*38A=	NP_001020332.2:n.*38A=