Canonical Allele Identifier: CA2649660790

Gene: ASPM

Linked Data

• gnomAD v4: 1-197090747-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090748_197090749del , CM000663.2:g.197090748_197090749del	GRCh38
NC_000001.10:g.197059878_197059879del , CM000663.1:g.197059878_197059879del	GRCh37
NC_000001.9:g.195326501_195326502del	NCBI36
NG_015867.1:g.60946_60947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2923+101_2923+102del
ENST00000367409.9:c.9636+101_9636+102del MANE Select	ENSP00000356379.4:n.9636+101_9636+102del
ENST00000680265.1:c.9858+101_9858+102del	ENSP00000505384.1:n.9858+101_9858+102del
ENST00000680710.1:c.9612+101_9612+102del	ENSP00000506676.1:n.9612+101_9612+102del
ENST00000294732.11:c.4881+101_4881+102del	ENSP00000294732.7:n.4881+101_4881+102del
ENST00000367408.5:c.2631+101_2631+102del	ENSP00000356378.1:n.2631+101_2631+102del
ENST00000367409.8:c.9636+101_9636+102del	ENSP00000356379.4:n.9636+101_9636+102del
ENST00000612785.1:c.3594+101_3594+102del	ENSP00000479244.1:n.3594+101_3594+102del
NM_001206846.1:c.4881+101_4881+102del	NP_001193775.1:n.4881+101_4881+102del
NM_018136.4:c.9636+101_9636+102del	NP_060606.3:n.9636+101_9636+102del
NM_018136.5:c.9636+101_9636+102del MANE Select	NP_060606.3:n.9636+101_9636+102del
NM_001206846.2:c.4881+101_4881+102del	NP_001193775.1:n.4881+101_4881+102del