Canonical Allele Identifier: CA2567213210
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197122625_197122626insTGGAATTCCTGTCCTGGCTCAGTGCAGACGAATCTGACTAGCTTCCATGAGGACAAAGTTTGGATCCCTGGCCT , CM000663.2:g.197122625_197122626insTGGAATTCCTGTCCTGGCTCAGTGCAGACGAATCTGACTAGCTTCCATGAGGACAAAGTTTGGATCCCTGGCCT GRCh38
NC_000001.10:g.197091755_197091756insTGGAATTCCTGTCCTGGCTCAGTGCAGACGAATCTGACTAGCTTCCATGAGGACAAAGTTTGGATCCCTGGCCT , CM000663.1:g.197091755_197091756insTGGAATTCCTGTCCTGGCTCAGTGCAGACGAATCTGACTAGCTTCCATGAGGACAAAGTTTGGATCCCTGGCCT GRCh37
NC_000001.9:g.195358378_195358379insTGGAATTCCTGTCCTGGCTCAGTGCAGACGAATCTGACTAGCTTCCATGAGGACAAAGTTTGGATCCCTGGCCT NCBI36
NG_015867.1:g.29069_29070insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1433-31_1433-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA
ENST00000367409.9:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA MANE Select ENSP00000356379.4:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000680112.1:n.1447-31_1447-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA
ENST00000680265.1:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000505384.1:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000680710.1:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000506676.1:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000681879.1:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000505363.1:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000294732.11:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000294732.7:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000367408.5:c.1141-31_1141-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000356378.1:n.1141-31_1141-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000367409.8:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000356379.4:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTC...
ENST00000612785.1:c.562-19979_562-19978insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA ENSP00000479244.1:n.562-19979_562-19978insAGGCCAGGGATCCAAACTT...
NM_001206846.1:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA NP_001193775.1:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTC...
NM_018136.4:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA NP_060606.3:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATG...
NM_018136.5:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA MANE Select NP_060606.3:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATG...
NM_001206846.2:c.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTCATGGAAGCTAGTCAGATTCGTCTGCACTGAGCCAGGACAGGAATTCCA NP_001193775.1:n.3391-31_3391-30insAGGCCAGGGATCCAAACTTTGTCCTC...