Canonical Allele Identifier: CA9695808
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231211G>T , CM000681.2:g.57231211G>T GRCh38
NC_000019.9:g.57742579G>T , CM000681.1:g.57742579G>T GRCh37
NC_000019.8:g.62434391G>T NCBI36
NG_012134.1:g.5203G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-38G>T MANE Select ENSP00000302898.6:n.-38G>T
ENST00000302804.11:c.-38G>T ENSP00000302898.6:n.-38G>T
ENST00000415300.6:c.1+97G>T ENSP00000407162.1:n.1+97G>T
ENST00000448930.5:c.-45+91G>T ENSP00000406798.2:n.-45+91G>T
ENST00000601799.5:c.-38G>T ENSP00000468918.1:n.-38G>T
NM_001015878.1:c.-38G>T NP_001015878.1:n.-38G>T
NM_001015879.1:c.1+97G>T NP_001015879.1:n.1+97G>T
NM_003160.2:c.-45+92G>T NP_003151.2:n.-45+92G>T
XR_430209.2:n.852G>T
XR_430209.3:n.895G>T
NM_001015878.2:c.-38G>T MANE Select NP_001015878.1:n.-38G>T
NM_001015879.2:c.1+97G>T NP_001015879.1:n.1+97G>T
NM_003160.3:c.-45+92G>T NP_003151.2:n.-45+92G>T