Canonical Allele Identifier: CA2344336885
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231104G= , CM000681.2:g.57231104G= GRCh38
NC_000019.9:g.57742472G= , CM000681.1:g.57742472G= GRCh37
NC_000019.8:g.62434284G= NCBI36
NG_012134.1:g.5096G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-145G= MANE Select ENSP00000302898.6:n.-145G=
ENST00000302804.11:c.-145G= ENSP00000302898.6:n.-145G=
ENST00000415300.6:c.-10G= ENSP00000407162.1:n.-10G=
ENST00000448930.5:c.-61G= ENSP00000406798.2:n.-61G=
NM_001015878.1:c.-145G= NP_001015878.1:n.-145G=
NM_001015879.1:c.-10G= NP_001015879.1:n.-10G=
NM_003160.2:c.-60G= NP_003151.2:n.-60G=
XR_430209.2:n.745G=
XR_430209.3:n.788G=
NM_001015878.2:c.-145G= MANE Select NP_001015878.1:n.-145G=
NM_001015879.2:c.-10G= NP_001015879.1:n.-10G=
NM_003160.3:c.-60G= NP_003151.2:n.-60G=