Canonical Allele Identifier: CA344014368
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs1195117565

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197101255T>C , CM000663.2:g.197101255T>C GRCh38
NC_000001.10:g.197070385T>C , CM000663.1:g.197070385T>C GRCh37
NC_000001.9:g.195337008T>C NCBI36
NG_015867.1:g.50440A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2108-5091A>G
ENST00000367409.9:c.7996A>G MANE Select ENSP00000356379.4:p.Thr2666Ala
ENST00000680265.1:c.7996A>G ENSP00000505384.1:p.Thr2666Ala
ENST00000680710.1:c.7996A>G ENSP00000506676.1:p.Thr2666Ala
ENST00000294732.11:c.4066-5091A>G ENSP00000294732.7:n.4066-5091A>G
ENST00000367408.5:c.1816-5091A>G ENSP00000356378.1:n.1816-5091A>G
ENST00000367409.8:c.7996A>G ENSP00000356379.4:p.Thr2666Ala
ENST00000612785.1:c.1954A>G ENSP00000479244.1:p.Thr652Ala
NM_001206846.1:c.4066-5091A>G NP_001193775.1:n.4066-5091A>G
NM_018136.4:c.7996A>G NP_060606.3:p.Thr2666Ala
NM_018136.5:c.7996A>G MANE Select NP_060606.3:p.Thr2666Ala
NM_001206846.2:c.4066-5091A>G NP_001193775.1:n.4066-5091A>G