Canonical Allele Identifier: CA407692522
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234895T>A , CM000681.2:g.57234895T>A GRCh38
NC_000019.9:g.57746263T>A , CM000681.1:g.57746263T>A GRCh37
NC_000019.8:g.62438075T>A NCBI36
NG_012134.1:g.8887T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.596T>A MANE Select ENSP00000302898.6:p.Met199Lys
ENST00000302804.11:c.596T>A ENSP00000302898.6:p.Met199Lys
ENST00000415300.6:c.539T>A ENSP00000407162.1:p.Met180Lys
ENST00000448930.5:c.491T>A ENSP00000406798.2:p.Met164Lys
ENST00000594599.1:c.80T>A ENSP00000469894.1:p.Met27Lys
ENST00000596375.1:c.*157T>A ENSP00000470465.1:n.*157T>A
ENST00000598785.5:c.494T>A ENSP00000471830.1:p.Met165Lys
ENST00000599062.5:c.587T>A ENSP00000469983.1:p.Met196Lys
ENST00000601799.5:c.*895T>A ENSP00000468918.1:n.*895T>A
NM_001015878.1:c.596T>A NP_001015878.1:p.Met199Lys
NM_001015879.1:c.539T>A NP_001015879.1:p.Met180Lys
NM_003160.2:c.494T>A NP_003151.2:p.Met165Lys
XR_430209.2:n.1490T>A
XR_430209.3:n.1533T>A
NM_001015878.2:c.596T>A MANE Select NP_001015878.1:p.Met199Lys
NM_001015879.2:c.539T>A NP_001015879.1:p.Met180Lys
NM_003160.3:c.494T>A NP_003151.2:p.Met165Lys