Canonical Allele Identifier: CA407693073
Gene: AURKC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57234981C>T , CM000681.2:g.57234981C>T GRCh38
NC_000019.9:g.57746349C>T , CM000681.1:g.57746349C>T GRCh37
NC_000019.8:g.62438161C>T NCBI36
NG_012134.1:g.8973C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.682C>T MANE Select ENSP00000302898.6:p.Leu228Phe
ENST00000302804.11:c.682C>T ENSP00000302898.6:p.Leu228Phe
ENST00000415300.6:c.625C>T ENSP00000407162.1:p.Leu209Phe
ENST00000448930.5:c.577C>T ENSP00000406798.2:p.Leu193Phe
ENST00000594599.1:c.166C>T ENSP00000469894.1:p.Leu56Phe
ENST00000596375.1:c.*243C>T ENSP00000470465.1:n.*243C>T
ENST00000598785.5:c.580C>T ENSP00000471830.1:p.Leu194Phe
ENST00000599062.5:c.673C>T ENSP00000469983.1:p.Leu225Phe
ENST00000601799.5:c.*981C>T ENSP00000468918.1:n.*981C>T
NM_001015878.1:c.682C>T NP_001015878.1:p.Leu228Phe
NM_001015879.1:c.625C>T NP_001015879.1:p.Leu209Phe
NM_003160.2:c.580C>T NP_003151.2:p.Leu194Phe
XR_430209.2:n.1576C>T
XR_430209.3:n.1619C>T
NM_001015878.2:c.682C>T MANE Select NP_001015878.1:p.Leu228Phe
NM_001015879.2:c.625C>T NP_001015879.1:p.Leu209Phe
NM_003160.3:c.580C>T NP_003151.2:p.Leu194Phe