Canonical Allele Identifier: CA407692951
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234955A>G , CM000681.2:g.57234955A>G GRCh38
NC_000019.9:g.57746323A>G , CM000681.1:g.57746323A>G GRCh37
NC_000019.8:g.62438135A>G NCBI36
NG_012134.1:g.8947A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.656A>G MANE Select ENSP00000302898.6:p.Lys219Arg
ENST00000302804.11:c.656A>G ENSP00000302898.6:p.Lys219Arg
ENST00000415300.6:c.599A>G ENSP00000407162.1:p.Lys200Arg
ENST00000448930.5:c.551A>G ENSP00000406798.2:p.Lys184Arg
ENST00000594599.1:c.140A>G ENSP00000469894.1:p.Lys47Arg
ENST00000596375.1:c.*217A>G ENSP00000470465.1:n.*217A>G
ENST00000598785.5:c.554A>G ENSP00000471830.1:p.Lys185Arg
ENST00000599062.5:c.647A>G ENSP00000469983.1:p.Lys216Arg
ENST00000601799.5:c.*955A>G ENSP00000468918.1:n.*955A>G
NM_001015878.1:c.656A>G NP_001015878.1:p.Lys219Arg
NM_001015879.1:c.599A>G NP_001015879.1:p.Lys200Arg
NM_003160.2:c.554A>G NP_003151.2:p.Lys185Arg
XR_430209.2:n.1550A>G
XR_430209.3:n.1593A>G
NM_001015878.2:c.656A>G MANE Select NP_001015878.1:p.Lys219Arg
NM_001015879.2:c.599A>G NP_001015879.1:p.Lys200Arg
NM_003160.3:c.554A>G NP_003151.2:p.Lys185Arg