Canonical Allele Identifier: CA407692447
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234886G>A , CM000681.2:g.57234886G>A GRCh38
NC_000019.9:g.57746254G>A , CM000681.1:g.57746254G>A GRCh37
NC_000019.8:g.62438066G>A NCBI36
NG_012134.1:g.8878G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.587G>A MANE Select ENSP00000302898.6:p.Arg196Lys
ENST00000302804.11:c.587G>A ENSP00000302898.6:p.Arg196Lys
ENST00000415300.6:c.530G>A ENSP00000407162.1:p.Arg177Lys
ENST00000448930.5:c.482G>A ENSP00000406798.2:p.Arg161Lys
ENST00000594599.1:c.71G>A ENSP00000469894.1:p.Arg24Lys
ENST00000596375.1:c.*148G>A ENSP00000470465.1:n.*148G>A
ENST00000598785.5:c.485G>A ENSP00000471830.1:p.Arg162Lys
ENST00000599062.5:c.578G>A ENSP00000469983.1:p.Arg193Lys
ENST00000601799.5:c.*886G>A ENSP00000468918.1:n.*886G>A
NM_001015878.1:c.587G>A NP_001015878.1:p.Arg196Lys
NM_001015879.1:c.530G>A NP_001015879.1:p.Arg177Lys
NM_003160.2:c.485G>A NP_003151.2:p.Arg162Lys
XR_430209.2:n.1481G>A
XR_430209.3:n.1524G>A
NM_001015878.2:c.587G>A MANE Select NP_001015878.1:p.Arg196Lys
NM_001015879.2:c.530G>A NP_001015879.1:p.Arg177Lys
NM_003160.3:c.485G>A NP_003151.2:p.Arg162Lys