Canonical Allele Identifier: CA2406579547

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128882T= , CM000684.2:g.42128882T=	GRCh38
NC_000022.10:g.42524884T= , CM000684.1:g.42524884T=	GRCh37
NC_000022.9:g.40854828T=	NCBI36
NG_008376.3:g.6110A=
NG_008376.4:g.6929A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.415A=	ENSP00000353241.6:p.Thr139=
ENST00000645361.2:c.568A= MANE Select	ENSP00000496150.1:p.Thr190=
ENST00000359033.4:c.415A=	ENSP00000351927.4:p.Thr139=
ENST00000360124.9:c.235A=	ENSP00000353241.5:p.Thr79=
ENST00000360608.9:c.568A=	ENSP00000353820.5:p.Thr190=
ENST00000389970.7:c.502A=	ENSP00000374620.4:p.Thr168=
ENST00000488442.1:n.1292A=
NM_000106.5:c.568A=	NP_000097.3:p.Thr190=
NM_001025161.2:c.415A=	NP_001020332.2:p.Thr139=
XM_011529966.1:c.568A=	XP_011528268.1:p.Thr190=
XM_011529967.1:c.568A=	XP_011528269.1:p.Thr190=
XM_011529968.1:c.568A=	XP_011528270.1:p.Thr190=
XM_011529969.1:c.424A=	XP_011528271.1:p.Thr142=
XM_011529970.1:c.415A=	XP_011528272.1:p.Thr139=
XM_011529971.1:c.424A=	XP_011528273.1:p.Thr142=
XM_011529972.1:c.568A=	XP_011528274.1:p.Thr190=
NM_000106.6:c.568A= MANE Select	NP_000097.3:p.Thr190=
NM_001025161.3:c.415A=	NP_001020332.2:p.Thr139=