Canonical Allele Identifier: CA2406577810

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126612T= , CM000684.2:g.42126612T=	GRCh38
NC_000022.10:g.42522614T= , CM000684.1:g.42522614T=	GRCh37
NC_000022.9:g.40852558T=	NCBI36
NG_008376.3:g.8380A=
NG_008376.4:g.9199A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1254A=	ENSP00000353241.6:n.1254A=
ENST00000645361.2:c.1456A= MANE Select	ENSP00000496150.1:p.Ser486=
ENST00000359033.4:c.1303A=	ENSP00000351927.4:p.Ser435=
ENST00000360124.9:c.1074A=	ENSP00000353241.5:n.1074A=
ENST00000360608.9:c.1456A=	ENSP00000353820.5:p.Ser486=
ENST00000389970.7:c.1447A=	ENSP00000374620.4:p.Ser483=
ENST00000488442.1:n.2180A=
NM_000106.5:c.1456A=	NP_000097.3:p.Ser486=
NM_001025161.2:c.1303A=	NP_001020332.2:p.Ser435=
XM_011529966.1:c.1452+4A=	XP_011528268.1:n.1452+4A=
XM_011529967.1:c.1452+4A=	XP_011528269.1:n.1452+4A=
XM_011529968.1:c.1452+4A=	XP_011528270.1:n.1452+4A=
XM_011529969.1:c.1308+4A=	XP_011528271.1:n.1308+4A=
XM_011529970.1:c.1299+4A=	XP_011528272.1:n.1299+4A=
XM_011529971.1:c.1312A=	XP_011528273.1:p.Ser438=
NM_000106.6:c.1456A= MANE Select	NP_000097.3:p.Ser486=
NM_001025161.3:c.1303A=	NP_001020332.2:p.Ser435=