Canonical Allele Identifier: CA1025922160

Gene: CYP2D6

Linked Data

• dbSNP Id: rs1931365063
• gnomAD v3: 22-42128500-C-CAT
• gnomAD v4: 22-42128500-C-CAT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128500_42128501insAT , CM000684.2:g.42128500_42128501insAT	GRCh38
NC_000022.10:g.42524502_42524503insAT , CM000684.1:g.42524502_42524503insAT	GRCh37
NC_000022.9:g.40854446_40854447insAT	NCBI36
NG_008376.3:g.6491_6492insAT
NG_008376.4:g.7310_7311insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.514-151_514-150insAT	ENSP00000353241.6:n.514-151_514-150insAT
ENST00000645361.2:c.667-151_667-150insAT MANE Select	ENSP00000496150.1:n.667-151_667-150insAT
ENST00000359033.4:c.514-151_514-150insAT	ENSP00000351927.4:n.514-151_514-150insAT
ENST00000360124.9:c.334-151_334-150insAT	ENSP00000353241.5:n.334-151_334-150insAT
ENST00000360608.9:c.667-151_667-150insAT	ENSP00000353820.5:n.667-151_667-150insAT
ENST00000389970.7:c.601-151_601-150insAT	ENSP00000374620.4:n.601-151_601-150insAT
ENST00000488442.1:n.1391-151_1391-150insAT
NM_000106.5:c.667-151_667-150insAT	NP_000097.3:n.667-151_667-150insAT
NM_001025161.2:c.514-151_514-150insAT	NP_001020332.2:n.514-151_514-150insAT
XM_011529966.1:c.667-151_667-150insAT	XP_011528268.1:n.667-151_667-150insAT
XM_011529967.1:c.667-151_667-150insAT	XP_011528269.1:n.667-151_667-150insAT
XM_011529968.1:c.667-151_667-150insAT	XP_011528270.1:n.667-151_667-150insAT
XM_011529969.1:c.523-151_523-150insAT	XP_011528271.1:n.523-151_523-150insAT
XM_011529970.1:c.514-151_514-150insAT	XP_011528272.1:n.514-151_514-150insAT
XM_011529971.1:c.523-151_523-150insAT	XP_011528273.1:n.523-151_523-150insAT
XM_011529972.1:c.667-151_667-150insAT	XP_011528274.1:n.667-151_667-150insAT
NM_000106.6:c.667-151_667-150insAT MANE Select	NP_000097.3:n.667-151_667-150insAT
NM_001025161.3:c.514-151_514-150insAT	NP_001020332.2:n.514-151_514-150insAT