Canonical Allele Identifier: CA9695807
Gene: AURKC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231169dup , CM000681.2:g.57231169dup GRCh38
NC_000019.9:g.57742537dup , CM000681.1:g.57742537dup GRCh37
NC_000019.8:g.62434349dup NCBI36
NG_012134.1:g.5161dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-80dup MANE Select ENSP00000302898.6:n.-80dup
ENST00000302804.11:c.-80dup ENSP00000302898.6:n.-80dup
ENST00000415300.6:c.1+55dup ENSP00000407162.1:n.1+55dup
ENST00000448930.5:c.-45+49dup ENSP00000406798.2:n.-45+49dup
ENST00000601799.5:c.-80dup ENSP00000468918.1:n.-80dup
NM_001015878.1:c.-80dup NP_001015878.1:n.-80dup
NM_001015879.1:c.1+55dup NP_001015879.1:n.1+55dup
NM_003160.2:c.-45+50dup NP_003151.2:n.-45+50dup
XR_430209.2:n.810dup
XR_430209.3:n.853dup
NM_001015878.2:c.-80dup MANE Select NP_001015878.1:n.-80dup
NM_001015879.2:c.1+55dup NP_001015879.1:n.1+55dup
NM_003160.3:c.-45+50dup NP_003151.2:n.-45+50dup