Canonical Allele Identifier: CA2344336896
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231116T= , CM000681.2:g.57231116T= GRCh38
NC_000019.9:g.57742484T= , CM000681.1:g.57742484T= GRCh37
NC_000019.8:g.62434296T= NCBI36
NG_012134.1:g.5108T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-133T= MANE Select ENSP00000302898.6:n.-133T=
ENST00000302804.11:c.-133T= ENSP00000302898.6:n.-133T=
ENST00000415300.6:c.1+2T= ENSP00000407162.1:n.1+2T=
ENST00000448930.5:c.-49T= ENSP00000406798.2:n.-49T=
NM_001015878.1:c.-133T= NP_001015878.1:n.-133T=
NM_001015879.1:c.1+2T= NP_001015879.1:n.1+2T=
NM_003160.2:c.-48T= NP_003151.2:n.-48T=
XR_430209.2:n.757T=
XR_430209.3:n.800T=
NM_001015878.2:c.-133T= MANE Select NP_001015878.1:n.-133T=
NM_001015879.2:c.1+2T= NP_001015879.1:n.1+2T=
NM_003160.3:c.-48T= NP_003151.2:n.-48T=