Canonical Allele Identifier: CA1217925090
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197090163C= , CM000663.2:g.197090163C= GRCh38
NC_000001.10:g.197059293C= , CM000663.1:g.197059293C= GRCh37
NC_000001.9:g.195325916C= NCBI36
NG_015867.1:g.61532G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.3116+33G=
ENST00000367409.9:c.9829+33G= MANE Select ENSP00000356379.4:n.9829+33G=
ENST00000680265.1:c.10051+33G= ENSP00000505384.1:n.10051+33G=
ENST00000680710.1:c.9805+33G= ENSP00000506676.1:n.9805+33G=
ENST00000294732.11:c.5074+33G= ENSP00000294732.7:n.5074+33G=
ENST00000367408.5:c.2824+33G= ENSP00000356378.1:n.2824+33G=
ENST00000367409.8:c.9829+33G= ENSP00000356379.4:n.9829+33G=
ENST00000612785.1:c.3787+33G= ENSP00000479244.1:n.3787+33G=
NM_001206846.1:c.5074+33G= NP_001193775.1:n.5074+33G=
NM_018136.4:c.9829+33G= NP_060606.3:n.9829+33G=
NM_018136.5:c.9829+33G= MANE Select NP_060606.3:n.9829+33G=
NM_001206846.2:c.5074+33G= NP_001193775.1:n.5074+33G=