Canonical Allele Identifier: CA407692463
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234888A>G , CM000681.2:g.57234888A>G GRCh38
NC_000019.9:g.57746256A>G , CM000681.1:g.57746256A>G GRCh37
NC_000019.8:g.62438068A>G NCBI36
NG_012134.1:g.8880A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.589A>G MANE Select ENSP00000302898.6:p.Lys197Glu
ENST00000302804.11:c.589A>G ENSP00000302898.6:p.Lys197Glu
ENST00000415300.6:c.532A>G ENSP00000407162.1:p.Lys178Glu
ENST00000448930.5:c.484A>G ENSP00000406798.2:p.Lys162Glu
ENST00000594599.1:c.73A>G ENSP00000469894.1:p.Lys25Glu
ENST00000596375.1:c.*150A>G ENSP00000470465.1:n.*150A>G
ENST00000598785.5:c.487A>G ENSP00000471830.1:p.Lys163Glu
ENST00000599062.5:c.580A>G ENSP00000469983.1:p.Lys194Glu
ENST00000601799.5:c.*888A>G ENSP00000468918.1:n.*888A>G
NM_001015878.1:c.589A>G NP_001015878.1:p.Lys197Glu
NM_001015879.1:c.532A>G NP_001015879.1:p.Lys178Glu
NM_003160.2:c.487A>G NP_003151.2:p.Lys163Glu
XR_430209.2:n.1483A>G
XR_430209.3:n.1526A>G
NM_001015878.2:c.589A>G MANE Select NP_001015878.1:p.Lys197Glu
NM_001015879.2:c.532A>G NP_001015879.1:p.Lys178Glu
NM_003160.3:c.487A>G NP_003151.2:p.Lys163Glu