Canonical Allele Identifier: CA2344338752

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234898G= , CM000681.2:g.57234898G=	GRCh38
NC_000019.9:g.57746266G= , CM000681.1:g.57746266G=	GRCh37
NC_000019.8:g.62438078G=	NCBI36
NG_012134.1:g.8890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.599G= MANE Select	ENSP00000302898.6:p.Cys200=
ENST00000302804.11:c.599G=	ENSP00000302898.6:p.Cys200=
ENST00000415300.6:c.542G=	ENSP00000407162.1:p.Cys181=
ENST00000448930.5:c.494G=	ENSP00000406798.2:p.Cys165=
ENST00000594599.1:c.83G=	ENSP00000469894.1:p.Cys28=
ENST00000596375.1:c.*160G=	ENSP00000470465.1:n.*160G=
ENST00000598785.5:c.497G=	ENSP00000471830.1:p.Cys166=
ENST00000599062.5:c.590G=	ENSP00000469983.1:p.Cys197=
ENST00000601799.5:c.*898G=	ENSP00000468918.1:n.*898G=
NM_001015878.1:c.599G=	NP_001015878.1:p.Cys200=
NM_001015879.1:c.542G=	NP_001015879.1:p.Cys181=
NM_003160.2:c.497G=	NP_003151.2:p.Cys166=
XR_430209.2:n.1493G=
XR_430209.3:n.1536G=
NM_001015878.2:c.599G= MANE Select	NP_001015878.1:p.Cys200=
NM_001015879.2:c.542G=	NP_001015879.1:p.Cys181=
NM_003160.3:c.497G=	NP_003151.2:p.Cys166=