Canonical Allele Identifier: CA1217945559
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197142655T= , CM000663.2:g.197142655T= GRCh38
NC_000001.10:g.197111785T= , CM000663.1:g.197111785T= GRCh37
NC_000001.9:g.195378408T= NCBI36
NG_015867.1:g.9040A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.1597A= MANE Select ENSP00000356379.4:p.Asn533=
ENST00000679766.1:n.1814A=
ENST00000680265.1:c.1597A= ENSP00000505384.1:p.Asn533=
ENST00000680710.1:c.1597A= ENSP00000506676.1:p.Asn533=
ENST00000681879.1:c.1597A= ENSP00000505363.1:p.Asn533=
ENST00000294732.11:c.1597A= ENSP00000294732.7:p.Asn533=
ENST00000367409.8:c.1597A= ENSP00000356379.4:p.Asn533=
ENST00000612785.1:c.561+1036A= ENSP00000479244.1:n.561+1036A=
NM_001206846.1:c.1597A= NP_001193775.1:p.Asn533=
NM_018136.4:c.1597A= NP_060606.3:p.Asn533=
NM_018136.5:c.1597A= MANE Select NP_060606.3:p.Asn533=
NM_001206846.2:c.1597A= NP_001193775.1:p.Asn533=