Canonical Allele Identifier: CA2344338749

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234890G= , CM000681.2:g.57234890G=	GRCh38
NC_000019.9:g.57746258G= , CM000681.1:g.57746258G=	GRCh37
NC_000019.8:g.62438070G=	NCBI36
NG_012134.1:g.8882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.591G= MANE Select	ENSP00000302898.6:p.Lys197=
ENST00000302804.11:c.591G=	ENSP00000302898.6:p.Lys197=
ENST00000415300.6:c.534G=	ENSP00000407162.1:p.Lys178=
ENST00000448930.5:c.486G=	ENSP00000406798.2:p.Lys162=
ENST00000594599.1:c.75G=	ENSP00000469894.1:p.Lys25=
ENST00000596375.1:c.*152G=	ENSP00000470465.1:n.*152G=
ENST00000598785.5:c.489G=	ENSP00000471830.1:p.Lys163=
ENST00000599062.5:c.582G=	ENSP00000469983.1:p.Lys194=
ENST00000601799.5:c.*890G=	ENSP00000468918.1:n.*890G=
NM_001015878.1:c.591G=	NP_001015878.1:p.Lys197=
NM_001015879.1:c.534G=	NP_001015879.1:p.Lys178=
NM_003160.2:c.489G=	NP_003151.2:p.Lys163=
XR_430209.2:n.1485G=
XR_430209.3:n.1528G=
NM_001015878.2:c.591G= MANE Select	NP_001015878.1:p.Lys197=
NM_001015879.2:c.534G=	NP_001015879.1:p.Lys178=
NM_003160.3:c.489G=	NP_003151.2:p.Lys163=