Canonical Allele Identifier: CA2580061806
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197143723del , CM000663.2:g.197143723del GRCh38
NC_000001.10:g.197112853del , CM000663.1:g.197112853del GRCh37
NC_000001.9:g.195379476del NCBI36
NG_015867.1:g.7975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367409.9:c.532del MANE Select ENSP00000356379.4:p.Thr178HisfsTer23
ENST00000679766.1:n.749del
ENST00000680265.1:c.532del ENSP00000505384.1:p.Thr178HisfsTer23
ENST00000680710.1:c.532del ENSP00000506676.1:p.Thr178HisfsTer23
ENST00000681879.1:c.532del ENSP00000505363.1:p.Thr178HisfsTer23
ENST00000294732.11:c.532del ENSP00000294732.7:p.Thr178HisfsTer23
ENST00000367409.8:c.532del ENSP00000356379.4:p.Thr178HisfsTer23
ENST00000612785.1:c.532del ENSP00000479244.1:p.Thr178HisfsTer21
NM_001206846.1:c.532del NP_001193775.1:p.Thr178HisfsTer23
NM_018136.4:c.532del NP_060606.3:p.Thr178HisfsTer23
NM_018136.5:c.532del MANE Select NP_060606.3:p.Thr178HisfsTer23
NM_001206846.2:c.532del NP_001193775.1:p.Thr178HisfsTer23