Canonical Allele Identifier: CA2344336895
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231115G= , CM000681.2:g.57231115G= GRCh38
NC_000019.9:g.57742483G= , CM000681.1:g.57742483G= GRCh37
NC_000019.8:g.62434295G= NCBI36
NG_012134.1:g.5107G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-134G= MANE Select ENSP00000302898.6:n.-134G=
ENST00000302804.11:c.-134G= ENSP00000302898.6:n.-134G=
ENST00000415300.6:c.1+1G= ENSP00000407162.1:n.1+1G=
ENST00000448930.5:c.-50G= ENSP00000406798.2:n.-50G=
NM_001015878.1:c.-134G= NP_001015878.1:n.-134G=
NM_001015879.1:c.1+1G= NP_001015879.1:n.1+1G=
NM_003160.2:c.-49G= NP_003151.2:n.-49G=
XR_430209.2:n.756G=
XR_430209.3:n.799G=
NM_001015878.2:c.-134G= MANE Select NP_001015878.1:n.-134G=
NM_001015879.2:c.1+1G= NP_001015879.1:n.1+1G=
NM_003160.3:c.-49G= NP_003151.2:n.-49G=