Canonical Allele Identifier: CA1217945841

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142845_197142850delinsATTATT , CM000663.2:g.197142845_197142850delinsATTATT	GRCh38
NC_000001.10:g.197111975_197111980delinsATTATT , CM000663.1:g.197111975_197111980delinsATTATT	GRCh37
NC_000001.9:g.195378598_195378603delinsATTATT	NCBI36
NG_015867.1:g.8845_8850delinsAATAAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367409.9:c.1402_1407delinsAATAAT MANE Select	ENSP00000356379.4:p.Asn468=
ENST00000679766.1:n.1619_1624delinsAATAAT
ENST00000680265.1:c.1402_1407delinsAATAAT	ENSP00000505384.1:p.Asn468=
ENST00000680710.1:c.1402_1407delinsAATAAT	ENSP00000506676.1:p.Asn468=
ENST00000681879.1:c.1402_1407delinsAATAAT	ENSP00000505363.1:p.Asn468=
ENST00000294732.11:c.1402_1407delinsAATAAT	ENSP00000294732.7:p.Asn468=
ENST00000367409.8:c.1402_1407delinsAATAAT	ENSP00000356379.4:p.Asn468=
ENST00000612785.1:c.561+841_561+846delinsAATAAT	ENSP00000479244.1:n.561+841_561+846delins...
NM_001206846.1:c.1402_1407delinsAATAAT	NP_001193775.1:p.Asn468=
NM_018136.4:c.1402_1407delinsAATAAT	NP_060606.3:p.Asn468=
NM_018136.5:c.1402_1407delinsAATAAT MANE Select	NP_060606.3:p.Asn468=
NM_001206846.2:c.1402_1407delinsAATAAT	NP_001193775.1:p.Asn468=