Canonical Allele Identifier: CA2406579204

Gene: CYP2D6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42128471_42128472delinsCA , CM000684.2:g.42128471_42128472delinsCA	GRCh38
NC_000022.10:g.42524473_42524474delinsCA , CM000684.1:g.42524473_42524474delinsCA	GRCh37
NC_000022.9:g.40854417_40854418delinsCA	NCBI36
NG_008376.3:g.6520_6521delinsTG
NG_008376.4:g.7339_7340delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360124.10:c.514-122_514-121delinsTG	ENSP00000353241.6:n.514-122_514-121delinsTG
ENST00000645361.2:c.667-122_667-121delinsTG MANE Select	ENSP00000496150.1:n.667-122_667-121delinsTG
ENST00000359033.4:c.514-122_514-121delinsTG	ENSP00000351927.4:n.514-122_514-121delinsTG
ENST00000360124.9:c.334-122_334-121delinsTG	ENSP00000353241.5:n.334-122_334-121delinsTG
ENST00000360608.9:c.667-122_667-121delinsTG	ENSP00000353820.5:n.667-122_667-121delinsTG
ENST00000389970.7:c.601-122_601-121delinsTG	ENSP00000374620.4:n.601-122_601-121delinsTG
ENST00000488442.1:n.1391-122_1391-121delinsTG
NM_000106.5:c.667-122_667-121delinsTG	NP_000097.3:n.667-122_667-121delinsTG
NM_001025161.2:c.514-122_514-121delinsTG	NP_001020332.2:n.514-122_514-121delinsTG
XM_011529966.1:c.667-122_667-121delinsTG	XP_011528268.1:n.667-122_667-121delinsTG
XM_011529967.1:c.667-122_667-121delinsTG	XP_011528269.1:n.667-122_667-121delinsTG
XM_011529968.1:c.667-122_667-121delinsTG	XP_011528270.1:n.667-122_667-121delinsTG
XM_011529969.1:c.523-122_523-121delinsTG	XP_011528271.1:n.523-122_523-121delinsTG
XM_011529970.1:c.514-122_514-121delinsTG	XP_011528272.1:n.514-122_514-121delinsTG
XM_011529971.1:c.523-122_523-121delinsTG	XP_011528273.1:n.523-122_523-121delinsTG
XM_011529972.1:c.667-122_667-121delinsTG	XP_011528274.1:n.667-122_667-121delinsTG
NM_000106.6:c.667-122_667-121delinsTG MANE Select	NP_000097.3:n.667-122_667-121delinsTG
NM_001025161.3:c.514-122_514-121delinsTG	NP_001020332.2:n.514-122_514-121delinsTG