Canonical Allele Identifier: CA2649661707

Gene: ASPM

Linked Data

• gnomAD v4: 1-197101048-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101049del , CM000663.2:g.197101049del	GRCh38
NC_000001.10:g.197070179del , CM000663.1:g.197070179del	GRCh37
NC_000001.9:g.195336802del	NCBI36
NG_015867.1:g.50646del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-4885del
ENST00000367409.9:c.8202del MANE Select	ENSP00000356379.4:p.Leu2736Ter
ENST00000680265.1:c.8202del	ENSP00000505384.1:p.Leu2736Ter
ENST00000680710.1:c.8202del	ENSP00000506676.1:p.Leu2736Ter
ENST00000294732.11:c.4066-4885del	ENSP00000294732.7:n.4066-4885del
ENST00000367408.5:c.1816-4885del	ENSP00000356378.1:n.1816-4885del
ENST00000367409.8:c.8202del	ENSP00000356379.4:p.Leu2736Ter
ENST00000612785.1:c.2160del	ENSP00000479244.1:p.Leu722Ter
NM_001206846.1:c.4066-4885del	NP_001193775.1:n.4066-4885del
NM_018136.4:c.8202del	NP_060606.3:p.Leu2736Ter
NM_018136.5:c.8202del MANE Select	NP_060606.3:p.Leu2736Ter
NM_001206846.2:c.4066-4885del	NP_001193775.1:n.4066-4885del