Canonical Allele Identifier: CA407692472
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234889A>G , CM000681.2:g.57234889A>G GRCh38
NC_000019.9:g.57746257A>G , CM000681.1:g.57746257A>G GRCh37
NC_000019.8:g.62438069A>G NCBI36
NG_012134.1:g.8881A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.590A>G MANE Select ENSP00000302898.6:p.Lys197Arg
ENST00000302804.11:c.590A>G ENSP00000302898.6:p.Lys197Arg
ENST00000415300.6:c.533A>G ENSP00000407162.1:p.Lys178Arg
ENST00000448930.5:c.485A>G ENSP00000406798.2:p.Lys162Arg
ENST00000594599.1:c.74A>G ENSP00000469894.1:p.Lys25Arg
ENST00000596375.1:c.*151A>G ENSP00000470465.1:n.*151A>G
ENST00000598785.5:c.488A>G ENSP00000471830.1:p.Lys163Arg
ENST00000599062.5:c.581A>G ENSP00000469983.1:p.Lys194Arg
ENST00000601799.5:c.*889A>G ENSP00000468918.1:n.*889A>G
NM_001015878.1:c.590A>G NP_001015878.1:p.Lys197Arg
NM_001015879.1:c.533A>G NP_001015879.1:p.Lys178Arg
NM_003160.2:c.488A>G NP_003151.2:p.Lys163Arg
XR_430209.2:n.1484A>G
XR_430209.3:n.1527A>G
NM_001015878.2:c.590A>G MANE Select NP_001015878.1:p.Lys197Arg
NM_001015879.2:c.533A>G NP_001015879.1:p.Lys178Arg
NM_003160.3:c.488A>G NP_003151.2:p.Lys163Arg