Canonical Allele Identifier: CA1217930726

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103561_197103562delinsTC , CM000663.2:g.197103561_197103562delinsTC	GRCh38
NC_000001.10:g.197072691_197072692delinsTC , CM000663.1:g.197072691_197072692delinsTC	GRCh37
NC_000001.9:g.195339314_195339315delinsTC	NCBI36
NG_015867.1:g.48133_48134delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7398_2108-7397delinsGA
ENST00000367409.9:c.5689_5690delinsGA MANE Select	ENSP00000356379.4:p.Glu1897=
ENST00000680265.1:c.5689_5690delinsGA	ENSP00000505384.1:p.Glu1897=
ENST00000680710.1:c.5689_5690delinsGA	ENSP00000506676.1:p.Glu1897=
ENST00000294732.11:c.4066-7398_4066-7397delinsGA	ENSP00000294732.7:n.4066-7398_4066-7397delinsGA
ENST00000367408.5:c.1816-7398_1816-7397delinsGA	ENSP00000356378.1:n.1816-7398_1816-7397delinsGA
ENST00000367409.8:c.5689_5690delinsGA	ENSP00000356379.4:p.Glu1897=
ENST00000612785.1:c.562-915_562-914delinsGA	ENSP00000479244.1:n.562-915_562-914delinsGA
NM_001206846.1:c.4066-7398_4066-7397delinsGA	NP_001193775.1:n.4066-7398_4066-7397delinsGA
NM_018136.4:c.5689_5690delinsGA	NP_060606.3:p.Glu1897=
NM_018136.5:c.5689_5690delinsGA MANE Select	NP_060606.3:p.Glu1897=
NM_001206846.2:c.4066-7398_4066-7397delinsGA	NP_001193775.1:n.4066-7398_4066-7397delinsGA