Canonical Allele Identifier: CA645523002

Gene: ASPM

Linked Data

• COSMIC: COSM5832444

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103643_197103644insATTC , CM000663.2:g.197103643_197103644insATTC	GRCh38
NC_000001.10:g.197072773_197072774insATTC , CM000663.1:g.197072773_197072774insATTC	GRCh37
NC_000001.9:g.195339396_195339397insATTC	NCBI36
NG_015867.1:g.48051_48052insGAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7480_2108-7479insGAAT
ENST00000367409.9:c.5607_5608insGAAT MANE Select	ENSP00000356379.4:p.His1870GlufsTer27
ENST00000680265.1:c.5607_5608insGAAT	ENSP00000505384.1:p.His1870GlufsTer27
ENST00000680710.1:c.5607_5608insGAAT	ENSP00000506676.1:p.His1870GlufsTer27
ENST00000294732.11:c.4066-7480_4066-7479insGAAT	ENSP00000294732.7:n.4066-7480_4066-7479insGAAT
ENST00000367408.5:c.1816-7480_1816-7479insGAAT	ENSP00000356378.1:n.1816-7480_1816-7479insGAAT
ENST00000367409.8:c.5607_5608insGAAT	ENSP00000356379.4:p.His1870GlufsTer27
ENST00000612785.1:c.562-997_562-996insGAAT	ENSP00000479244.1:n.562-997_562-996insGAAT
NM_001206846.1:c.4066-7480_4066-7479insGAAT	NP_001193775.1:n.4066-7480_4066-7479insGAAT
NM_018136.4:c.5607_5608insGAAT	NP_060606.3:p.His1870GlufsTer27
NM_018136.5:c.5607_5608insGAAT MANE Select	NP_060606.3:p.His1870GlufsTer27
NM_001206846.2:c.4066-7480_4066-7479insGAAT	NP_001193775.1:n.4066-7480_4066-7479insGAAT