Canonical Allele Identifier: CA35873594
Gene: ASPM HGNC NCBI

Linked Data

ClinVar Variation Id: 2471935
ClinVar RCV Id: RCV003202846
dbSNP Id: rs934818920

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197103631T>C , CM000663.2:g.197103631T>C GRCh38
NC_000001.10:g.197072761T>C , CM000663.1:g.197072761T>C GRCh37
NC_000001.9:g.195339384T>C NCBI36
NG_015867.1:g.48064A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-7467A>G
ENST00000367409.9:c.5620A>G MANE Select ENSP00000356379.4:p.Thr1874Ala
ENST00000680265.1:c.5620A>G ENSP00000505384.1:p.Thr1874Ala
ENST00000680710.1:c.5620A>G ENSP00000506676.1:p.Thr1874Ala
ENST00000294732.11:c.4066-7467A>G ENSP00000294732.7:n.4066-7467A>G
ENST00000367408.5:c.1816-7467A>G ENSP00000356378.1:n.1816-7467A>G
ENST00000367409.8:c.5620A>G ENSP00000356379.4:p.Thr1874Ala
ENST00000612785.1:c.562-984A>G ENSP00000479244.1:n.562-984A>G
NM_001206846.1:c.4066-7467A>G NP_001193775.1:n.4066-7467A>G
NM_018136.4:c.5620A>G NP_060606.3:p.Thr1874Ala
NM_018136.5:c.5620A>G MANE Select NP_060606.3:p.Thr1874Ala
NM_001206846.2:c.4066-7467A>G NP_001193775.1:n.4066-7467A>G