Canonical Allele Identifier: CA407692884
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234943C>A , CM000681.2:g.57234943C>A GRCh38
NC_000019.9:g.57746311C>A , CM000681.1:g.57746311C>A GRCh37
NC_000019.8:g.62438123C>A NCBI36
NG_012134.1:g.8935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.644C>A MANE Select ENSP00000302898.6:p.Thr215Lys
ENST00000302804.11:c.644C>A ENSP00000302898.6:p.Thr215Lys
ENST00000415300.6:c.587C>A ENSP00000407162.1:p.Thr196Lys
ENST00000448930.5:c.539C>A ENSP00000406798.2:p.Thr180Lys
ENST00000594599.1:c.128C>A ENSP00000469894.1:p.Thr43Lys
ENST00000596375.1:c.*205C>A ENSP00000470465.1:n.*205C>A
ENST00000598785.5:c.542C>A ENSP00000471830.1:p.Thr181Lys
ENST00000599062.5:c.635C>A ENSP00000469983.1:p.Thr212Lys
ENST00000601799.5:c.*943C>A ENSP00000468918.1:n.*943C>A
NM_001015878.1:c.644C>A NP_001015878.1:p.Thr215Lys
NM_001015879.1:c.587C>A NP_001015879.1:p.Thr196Lys
NM_003160.2:c.542C>A NP_003151.2:p.Thr181Lys
XR_430209.2:n.1538C>A
XR_430209.3:n.1581C>A
NM_001015878.2:c.644C>A MANE Select NP_001015878.1:p.Thr215Lys
NM_001015879.2:c.587C>A NP_001015879.1:p.Thr196Lys
NM_003160.3:c.542C>A NP_003151.2:p.Thr181Lys