Canonical Allele Identifier: CA2406577890

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1930968102

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42126750_42126752dup , CM000684.2:g.42126750_42126752dup	GRCh38
NC_000022.10:g.42522752_42522754dup , CM000684.1:g.42522752_42522754dup	GRCh37
NC_000022.9:g.40852696_40852698dup	NCBI36
NG_008376.3:g.8244_8246dup
NG_008376.4:g.9063_9065dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000360124.10:c.1118_1120dup	ENSP00000353241.6:n.1118_1120dup
ENST00000645361.2:c.1320_1322dup MANE Select	ENSP00000496150.1:p.Arg441_Ala442insArg
ENST00000359033.4:c.1167_1169dup	ENSP00000351927.4:p.Arg390_Ala391insArg
ENST00000360124.9:c.938_940dup	ENSP00000353241.5:n.938_940dup
ENST00000360608.9:c.1320_1322dup	ENSP00000353820.5:p.Arg441_Ala442insArg
ENST00000389970.7:c.1311_1313dup	ENSP00000374620.4:p.Arg438_Ala439insArg
ENST00000488442.1:n.2044_2046dup
NM_000106.5:c.1320_1322dup	NP_000097.3:p.Arg441_Ala442insArg
NM_001025161.2:c.1167_1169dup	NP_001020332.2:p.Arg390_Ala391insArg
XM_011529966.1:c.1320_1322dup	XP_011528268.1:p.Arg441_Ala442insArg
XM_011529967.1:c.1320_1322dup	XP_011528269.1:p.Arg441_Ala442insArg
XM_011529968.1:c.1320_1322dup	XP_011528270.1:p.Arg441_Ala442insArg
XM_011529969.1:c.1176_1178dup	XP_011528271.1:p.Arg393_Ala394insArg
XM_011529970.1:c.1167_1169dup	XP_011528272.1:p.Arg390_Ala391insArg
XM_011529971.1:c.1176_1178dup	XP_011528273.1:p.Arg393_Ala394insArg
NM_000106.6:c.1320_1322dup MANE Select	NP_000097.3:p.Arg441_Ala442insArg
NM_001025161.3:c.1167_1169dup	NP_001020332.2:p.Arg390_Ala391insArg