Canonical Allele Identifier: CA920373725

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1465361319

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42130568_42130569del , CM000684.2:g.42130568_42130569del	GRCh38
NG_008376.3:g.4425_4426del
NG_008376.4:g.5244_5245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.180+45_180+46del	ENSP00000353241.6:n.180+45_180+46del
ENST00000645361.2:c.180+45_180+46del MANE Select	ENSP00000496150.1:n.180+45_180+46del
ENST00000359033.4:c.180+45_180+46del	ENSP00000351927.4:n.180+45_180+46del
ENST00000360608.9:c.180+45_180+46del	ENSP00000353820.5:n.180+45_180+46del
ENST00000389970.7:c.114+45_114+46del	ENSP00000374620.4:n.114+45_114+46del
ENST00000488442.1:n.247_248del
NM_000106.5:c.180+45_180+46del	NP_000097.3:n.180+45_180+46del
NM_001025161.2:c.180+45_180+46del	NP_001020332.2:n.180+45_180+46del
XM_011529966.1:c.180+45_180+46del	XP_011528268.1:n.180+45_180+46del
XM_011529967.1:c.180+45_180+46del	XP_011528269.1:n.180+45_180+46del
XM_011529968.1:c.180+45_180+46del	XP_011528270.1:n.180+45_180+46del
XM_011529969.1:c.38-658_38-657del	XP_011528271.1:n.38-658_38-657del
XM_011529970.1:c.180+45_180+46del	XP_011528272.1:n.180+45_180+46del
XM_011529971.1:c.38-658_38-657del	XP_011528273.1:n.38-658_38-657del
XM_011529972.1:c.180+45_180+46del	XP_011528274.1:n.180+45_180+46del
XR_430455.2:n.208_209del
NM_000106.6:c.180+45_180+46del MANE Select	NP_000097.3:n.180+45_180+46del
XR_002958749.1:n.155_156del
NM_001025161.3:c.180+45_180+46del	NP_001020332.2:n.180+45_180+46del