Canonical Allele Identifier: CA1217925295
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197090329T= , CM000663.2:g.197090329T= GRCh38
NC_000001.10:g.197059459T= , CM000663.1:g.197059459T= GRCh37
NC_000001.9:g.195326082T= NCBI36
NG_015867.1:g.61366A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2983A=
ENST00000367409.9:c.9696A= MANE Select ENSP00000356379.4:p.Ile3232=
ENST00000680265.1:c.9918A= ENSP00000505384.1:p.Ile3306=
ENST00000680710.1:c.9672A= ENSP00000506676.1:p.Ile3224=
ENST00000294732.11:c.4941A= ENSP00000294732.7:p.Ile1647=
ENST00000367408.5:c.2691A= ENSP00000356378.1:p.Ile897=
ENST00000367409.8:c.9696A= ENSP00000356379.4:p.Ile3232=
ENST00000612785.1:c.3654A= ENSP00000479244.1:p.Ile1218=
NM_001206846.1:c.4941A= NP_001193775.1:p.Ile1647=
NM_018136.4:c.9696A= NP_060606.3:p.Ile3232=
NM_018136.5:c.9696A= MANE Select NP_060606.3:p.Ile3232=
NM_001206846.2:c.4941A= NP_001193775.1:p.Ile1647=