Canonical Allele Identifier: CA9695837
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231699C>G , CM000681.2:g.57231699C>G GRCh38
NC_000019.9:g.57743067C>G , CM000681.1:g.57743067C>G GRCh37
NC_000019.8:g.62434879C>G NCBI36
NG_012134.1:g.5691C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.59-43C>G MANE Select ENSP00000302898.6:n.59-43C>G
ENST00000302804.11:c.59-43C>G ENSP00000302898.6:n.59-43C>G
ENST00000415300.6:c.2-43C>G ENSP00000407162.1:n.2-43C>G
ENST00000448930.5:c.-44-43C>G ENSP00000406798.2:n.-44-43C>G
ENST00000598785.5:c.-87C>G ENSP00000471830.1:n.-87C>G
ENST00000599062.5:c.59-52C>G ENSP00000469983.1:n.59-52C>G
ENST00000601799.5:c.*310C>G ENSP00000468918.1:n.*310C>G
NM_001015878.1:c.59-43C>G NP_001015878.1:n.59-43C>G
NM_001015879.1:c.2-43C>G NP_001015879.1:n.2-43C>G
NM_003160.2:c.-44-43C>G NP_003151.2:n.-44-43C>G
XR_430209.2:n.948-43C>G
XR_430209.3:n.991-43C>G
NM_001015878.2:c.59-43C>G MANE Select NP_001015878.1:n.59-43C>G
NM_001015879.2:c.2-43C>G NP_001015879.1:n.2-43C>G
NM_003160.3:c.-44-43C>G NP_003151.2:n.-44-43C>G