Canonical Allele Identifier: CA1217930065
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101773A= , CM000663.2:g.197101773A= GRCh38
NC_000001.10:g.197070903A= , CM000663.1:g.197070903A= GRCh37
NC_000001.9:g.195337526A= NCBI36
NG_015867.1:g.49922T=

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-5609T=
ENST00000367409.9:c.7478T= MANE Select ENSP00000356379.4:p.Met2493=
ENST00000680265.1:c.7478T= ENSP00000505384.1:p.Met2493=
ENST00000680710.1:c.7478T= ENSP00000506676.1:p.Met2493=
ENST00000294732.11:c.4066-5609T= ENSP00000294732.7:n.4066-5609T=
ENST00000367408.5:c.1816-5609T= ENSP00000356378.1:n.1816-5609T=
ENST00000367409.8:c.7478T= ENSP00000356379.4:p.Met2493=
ENST00000612785.1:c.1436T= ENSP00000479244.1:p.Met479=
NM_001206846.1:c.4066-5609T= NP_001193775.1:n.4066-5609T=
NM_018136.4:c.7478T= NP_060606.3:p.Met2493=
NM_018136.5:c.7478T= MANE Select NP_060606.3:p.Met2493=
NM_001206846.2:c.4066-5609T= NP_001193775.1:n.4066-5609T=