Canonical Allele Identifier: CA2344338751

Gene: AURKC

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.596T= MANE Select	ENSP00000302898.6:p.Met199=
ENST00000302804.11:c.596T=	ENSP00000302898.6:p.Met199=
ENST00000415300.6:c.539T=	ENSP00000407162.1:p.Met180=
ENST00000448930.5:c.491T=	ENSP00000406798.2:p.Met164=
ENST00000594599.1:c.80T=	ENSP00000469894.1:p.Met27=
ENST00000596375.1:c.*157T=	ENSP00000470465.1:n.*157T=
ENST00000598785.5:c.494T=	ENSP00000471830.1:p.Met165=
ENST00000599062.5:c.587T=	ENSP00000469983.1:p.Met196=
ENST00000601799.5:c.*895T=	ENSP00000468918.1:n.*895T=
NM_001015878.1:c.596T=	NP_001015878.1:p.Met199=
NM_001015879.1:c.539T=	NP_001015879.1:p.Met180=
NM_003160.2:c.494T=	NP_003151.2:p.Met165=
XR_430209.2:n.1490T=
XR_430209.3:n.1533T=
NM_001015878.2:c.596T= MANE Select	NP_001015878.1:p.Met199=
NM_001015879.2:c.539T=	NP_001015879.1:p.Met180=
NM_003160.3:c.494T=	NP_003151.2:p.Met165=