Canonical Allele Identifier: CA344003606
Gene: ASPM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197091014T>G , CM000663.2:g.197091014T>G GRCh38
NC_000001.10:g.197060144T>G , CM000663.1:g.197060144T>G GRCh37
NC_000001.9:g.195326767T>G NCBI36
NG_015867.1:g.60681A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2759A>C
ENST00000367409.9:c.9472A>C MANE Select ENSP00000356379.4:p.Lys3158Gln
ENST00000680265.1:c.9694A>C ENSP00000505384.1:p.Lys3232Gln
ENST00000680710.1:c.9448A>C ENSP00000506676.1:p.Lys3150Gln
ENST00000294732.11:c.4717A>C ENSP00000294732.7:p.Lys1573Gln
ENST00000367408.5:c.2467A>C ENSP00000356378.1:p.Lys823Gln
ENST00000367409.8:c.9472A>C ENSP00000356379.4:p.Lys3158Gln
ENST00000612785.1:c.3430A>C ENSP00000479244.1:p.Lys1144Gln
NM_001206846.1:c.4717A>C NP_001193775.1:p.Lys1573Gln
NM_018136.4:c.9472A>C NP_060606.3:p.Lys3158Gln
NM_018136.5:c.9472A>C MANE Select NP_060606.3:p.Lys3158Gln
NM_001206846.2:c.4717A>C NP_001193775.1:p.Lys1573Gln