Canonical Allele Identifier: CA1217925839
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197090978_197090979delinsTC , CM000663.2:g.197090978_197090979delinsTC GRCh38
NC_000001.10:g.197060108_197060109delinsTC , CM000663.1:g.197060108_197060109delinsTC GRCh37
NC_000001.9:g.195326731_195326732delinsTC NCBI36
NG_015867.1:g.60716_60717delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2794_2795delinsGA
ENST00000367409.9:c.9507_9508delinsGA MANE Select ENSP00000356379.4:p.Lys3169=
ENST00000680265.1:c.9729_9730delinsGA ENSP00000505384.1:p.Lys3243=
ENST00000680710.1:c.9483_9484delinsGA ENSP00000506676.1:p.Lys3161=
ENST00000294732.11:c.4752_4753delinsGA ENSP00000294732.7:p.Lys1584=
ENST00000367408.5:c.2502_2503delinsGA ENSP00000356378.1:p.Lys834=
ENST00000367409.8:c.9507_9508delinsGA ENSP00000356379.4:p.Lys3169=
ENST00000612785.1:c.3465_3466delinsGA ENSP00000479244.1:p.Lys1155=
NM_001206846.1:c.4752_4753delinsGA NP_001193775.1:p.Lys1584=
NM_018136.4:c.9507_9508delinsGA NP_060606.3:p.Lys3169=
NM_018136.5:c.9507_9508delinsGA MANE Select NP_060606.3:p.Lys3169=
NM_001206846.2:c.4752_4753delinsGA NP_001193775.1:p.Lys1584=