Canonical Allele Identifier: CA2406580994

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130565_42130567delinsAGG , CM000684.2:g.42130565_42130567delinsAGG	GRCh38
NG_008376.3:g.4425_4427delinsCCT
NG_008376.4:g.5244_5246delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+45_180+47delinsCCT	ENSP00000353241.6:n.180+45_180+47delinsCCT
ENST00000645361.2:c.180+45_180+47delinsCCT MANE Select	ENSP00000496150.1:n.180+45_180+47delinsCCT
ENST00000359033.4:c.180+45_180+47delinsCCT	ENSP00000351927.4:n.180+45_180+47delinsCCT
ENST00000360608.9:c.180+45_180+47delinsCCT	ENSP00000353820.5:n.180+45_180+47delinsCCT
ENST00000389970.7:c.114+45_114+47delinsCCT	ENSP00000374620.4:n.114+45_114+47delinsCCT
ENST00000488442.1:n.247_249delinsCCT
NM_000106.5:c.180+45_180+47delinsCCT	NP_000097.3:n.180+45_180+47delinsCCT
NM_001025161.2:c.180+45_180+47delinsCCT	NP_001020332.2:n.180+45_180+47delinsCCT
XM_011529966.1:c.180+45_180+47delinsCCT	XP_011528268.1:n.180+45_180+47delinsCCT
XM_011529967.1:c.180+45_180+47delinsCCT	XP_011528269.1:n.180+45_180+47delinsCCT
XM_011529968.1:c.180+45_180+47delinsCCT	XP_011528270.1:n.180+45_180+47delinsCCT
XM_011529969.1:c.38-658_38-656delinsCCT	XP_011528271.1:n.38-658_38-656delinsCCT
XM_011529970.1:c.180+45_180+47delinsCCT	XP_011528272.1:n.180+45_180+47delinsCCT
XM_011529971.1:c.38-658_38-656delinsCCT	XP_011528273.1:n.38-658_38-656delinsCCT
XM_011529972.1:c.180+45_180+47delinsCCT	XP_011528274.1:n.180+45_180+47delinsCCT
XR_430455.2:n.207-2_207delinsAGG
NM_000106.6:c.180+45_180+47delinsCCT MANE Select	NP_000097.3:n.180+45_180+47delinsCCT
XR_002958749.1:n.154-2_154delinsAGG
NM_001025161.3:c.180+45_180+47delinsCCT	NP_001020332.2:n.180+45_180+47delinsCCT