Canonical Allele Identifier: CA2840769014

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126582dup , CM000684.2:g.42126582dup	GRCh38
NC_000022.10:g.42522584dup , CM000684.1:g.42522584dup	GRCh37
NC_000022.9:g.40852528dup	NCBI36
NG_008376.3:g.8413dup
NG_008376.4:g.9232dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.1287dup	ENSP00000353241.6:n.1287dup
ENST00000645361.2:c.1489dup MANE Select	ENSP00000496150.1:p.Arg497ProfsTer7
ENST00000359033.4:c.1336dup	ENSP00000351927.4:p.Arg446ProfsTer7
ENST00000360124.9:c.1107dup	ENSP00000353241.5:n.1107dup
ENST00000360608.9:c.1489dup	ENSP00000353820.5:p.Arg497ProfsTer7
ENST00000389970.7:c.1480dup	ENSP00000374620.4:p.Arg494ProfsTer7
ENST00000488442.1:n.2213dup
NM_000106.5:c.1489dup	NP_000097.3:p.Arg497ProfsTer7
NM_001025161.2:c.1336dup	NP_001020332.2:p.Arg446ProfsTer7
XM_011529966.1:c.1452+37dup	XP_011528268.1:n.1452+37dup
XM_011529967.1:c.1452+37dup	XP_011528269.1:n.1452+37dup
XM_011529968.1:c.1452+37dup	XP_011528270.1:n.1452+37dup
XM_011529969.1:c.1308+37dup	XP_011528271.1:n.1308+37dup
XM_011529970.1:c.1299+37dup	XP_011528272.1:n.1299+37dup
XM_011529971.1:c.1345dup	XP_011528273.1:p.Arg449ProfsTer7
NM_000106.6:c.1489dup MANE Select	NP_000097.3:p.Arg497ProfsTer7
NM_001025161.3:c.1336dup	NP_001020332.2:p.Arg446ProfsTer7