Canonical Allele Identifier: CA344013913
Gene: ASPM HGNC NCBI

Linked Data

COSMIC: COSM901663

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101063T>G , CM000663.2:g.197101063T>G GRCh38
NC_000001.10:g.197070193T>G , CM000663.1:g.197070193T>G GRCh37
NC_000001.9:g.195336816T>G NCBI36
NG_015867.1:g.50632A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-4899A>C
ENST00000367409.9:c.8188A>C MANE Select ENSP00000356379.4:p.Thr2730Pro
ENST00000680265.1:c.8188A>C ENSP00000505384.1:p.Thr2730Pro
ENST00000680710.1:c.8188A>C ENSP00000506676.1:p.Thr2730Pro
ENST00000294732.11:c.4066-4899A>C ENSP00000294732.7:n.4066-4899A>C
ENST00000367408.5:c.1816-4899A>C ENSP00000356378.1:n.1816-4899A>C
ENST00000367409.8:c.8188A>C ENSP00000356379.4:p.Thr2730Pro
ENST00000612785.1:c.2146A>C ENSP00000479244.1:p.Thr716Pro
NM_001206846.1:c.4066-4899A>C NP_001193775.1:n.4066-4899A>C
NM_018136.4:c.8188A>C NP_060606.3:p.Thr2730Pro
NM_018136.5:c.8188A>C MANE Select NP_060606.3:p.Thr2730Pro
NM_001206846.2:c.4066-4899A>C NP_001193775.1:n.4066-4899A>C