Canonical Allele Identifier: CA407692944
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234954A>T , CM000681.2:g.57234954A>T GRCh38
NC_000019.9:g.57746322A>T , CM000681.1:g.57746322A>T GRCh37
NC_000019.8:g.62438134A>T NCBI36
NG_012134.1:g.8946A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.655A>T MANE Select ENSP00000302898.6:p.Lys219Ter
ENST00000302804.11:c.655A>T ENSP00000302898.6:p.Lys219Ter
ENST00000415300.6:c.598A>T ENSP00000407162.1:p.Lys200Ter
ENST00000448930.5:c.550A>T ENSP00000406798.2:p.Lys184Ter
ENST00000594599.1:c.139A>T ENSP00000469894.1:p.Lys47Ter
ENST00000596375.1:c.*216A>T ENSP00000470465.1:n.*216A>T
ENST00000598785.5:c.553A>T ENSP00000471830.1:p.Lys185Ter
ENST00000599062.5:c.646A>T ENSP00000469983.1:p.Lys216Ter
ENST00000601799.5:c.*954A>T ENSP00000468918.1:n.*954A>T
NM_001015878.1:c.655A>T NP_001015878.1:p.Lys219Ter
NM_001015879.1:c.598A>T NP_001015879.1:p.Lys200Ter
NM_003160.2:c.553A>T NP_003151.2:p.Lys185Ter
XR_430209.2:n.1549A>T
XR_430209.3:n.1592A>T
NM_001015878.2:c.655A>T MANE Select NP_001015878.1:p.Lys219Ter
NM_001015879.2:c.598A>T NP_001015879.1:p.Lys200Ter
NM_003160.3:c.553A>T NP_003151.2:p.Lys185Ter