Canonical Allele Identifier: CA1217945818
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142838_197142846delinsATTTAGGAT , CM000663.2:g.197142838_197142846delinsATTTAGGAT GRCh38
NC_000001.10:g.197111968_197111976delinsATTTAGGAT , CM000663.1:g.197111968_197111976delinsATTTAGGAT GRCh37
NC_000001.9:g.195378591_195378599delinsATTTAGGAT NCBI36
NG_015867.1:g.8849_8857delinsATCCTAAAT

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1406_1414delinsATCCTAAAT MANE Select ENSP00000356379.4:p.Asn469=
ENST00000679766.1:n.1623_1631delinsATCCTAAAT
ENST00000680265.1:c.1406_1414delinsATCCTAAAT ENSP00000505384.1:p.Asn469=
ENST00000680710.1:c.1406_1414delinsATCCTAAAT ENSP00000506676.1:p.Asn469=
ENST00000681879.1:c.1406_1414delinsATCCTAAAT ENSP00000505363.1:p.Asn469=
ENST00000294732.11:c.1406_1414delinsATCCTAAAT ENSP00000294732.7:p.Asn469=
ENST00000367409.8:c.1406_1414delinsATCCTAAAT ENSP00000356379.4:p.Asn469=
ENST00000612785.1:c.561+845_561+853delinsATCCTAAAT ENSP00000479244.1:n.561+845_561+853delins...
NM_001206846.1:c.1406_1414delinsATCCTAAAT NP_001193775.1:p.Asn469=
NM_018136.4:c.1406_1414delinsATCCTAAAT NP_060606.3:p.Asn469=
NM_018136.5:c.1406_1414delinsATCCTAAAT MANE Select NP_060606.3:p.Asn469=
NM_001206846.2:c.1406_1414delinsATCCTAAAT NP_001193775.1:p.Asn469=