Canonical Allele Identifier: CA1217930763

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103653_197103654delinsAT , CM000663.2:g.197103653_197103654delinsAT	GRCh38
NC_000001.10:g.197072783_197072784delinsAT , CM000663.1:g.197072783_197072784delinsAT	GRCh37
NC_000001.9:g.195339406_195339407delinsAT	NCBI36
NG_015867.1:g.48041_48042delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7490_2108-7489delinsAT
ENST00000367409.9:c.5597_5598delinsAT MANE Select	ENSP00000356379.4:p.Asp1866=
ENST00000680265.1:c.5597_5598delinsAT	ENSP00000505384.1:p.Asp1866=
ENST00000680710.1:c.5597_5598delinsAT	ENSP00000506676.1:p.Asp1866=
ENST00000294732.11:c.4066-7490_4066-7489delinsAT	ENSP00000294732.7:n.4066-7490_4066-7489delinsAT
ENST00000367408.5:c.1816-7490_1816-7489delinsAT	ENSP00000356378.1:n.1816-7490_1816-7489delinsAT
ENST00000367409.8:c.5597_5598delinsAT	ENSP00000356379.4:p.Asp1866=
ENST00000612785.1:c.562-1007_562-1006delinsAT	ENSP00000479244.1:n.562-1007_562-1006delinsAT
NM_001206846.1:c.4066-7490_4066-7489delinsAT	NP_001193775.1:n.4066-7490_4066-7489delinsAT
NM_018136.4:c.5597_5598delinsAT	NP_060606.3:p.Asp1866=
NM_018136.5:c.5597_5598delinsAT MANE Select	NP_060606.3:p.Asp1866=
NM_001206846.2:c.4066-7490_4066-7489delinsAT	NP_001193775.1:n.4066-7490_4066-7489delinsAT