Canonical Allele Identifier: CA407692478
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234890G>C , CM000681.2:g.57234890G>C GRCh38
NC_000019.9:g.57746258G>C , CM000681.1:g.57746258G>C GRCh37
NC_000019.8:g.62438070G>C NCBI36
NG_012134.1:g.8882G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.591G>C MANE Select ENSP00000302898.6:p.Lys197Asn
ENST00000302804.11:c.591G>C ENSP00000302898.6:p.Lys197Asn
ENST00000415300.6:c.534G>C ENSP00000407162.1:p.Lys178Asn
ENST00000448930.5:c.486G>C ENSP00000406798.2:p.Lys162Asn
ENST00000594599.1:c.75G>C ENSP00000469894.1:p.Lys25Asn
ENST00000596375.1:c.*152G>C ENSP00000470465.1:n.*152G>C
ENST00000598785.5:c.489G>C ENSP00000471830.1:p.Lys163Asn
ENST00000599062.5:c.582G>C ENSP00000469983.1:p.Lys194Asn
ENST00000601799.5:c.*890G>C ENSP00000468918.1:n.*890G>C
NM_001015878.1:c.591G>C NP_001015878.1:p.Lys197Asn
NM_001015879.1:c.534G>C NP_001015879.1:p.Lys178Asn
NM_003160.2:c.489G>C NP_003151.2:p.Lys163Asn
XR_430209.2:n.1485G>C
XR_430209.3:n.1528G>C
NM_001015878.2:c.591G>C MANE Select NP_001015878.1:p.Lys197Asn
NM_001015879.2:c.534G>C NP_001015879.1:p.Lys178Asn
NM_003160.3:c.489G>C NP_003151.2:p.Lys163Asn