Canonical Allele Identifier: CA2344338748

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234889A= , CM000681.2:g.57234889A=	GRCh38
NC_000019.9:g.57746257A= , CM000681.1:g.57746257A=	GRCh37
NC_000019.8:g.62438069A=	NCBI36
NG_012134.1:g.8881A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.590A= MANE Select	ENSP00000302898.6:p.Lys197=
ENST00000302804.11:c.590A=	ENSP00000302898.6:p.Lys197=
ENST00000415300.6:c.533A=	ENSP00000407162.1:p.Lys178=
ENST00000448930.5:c.485A=	ENSP00000406798.2:p.Lys162=
ENST00000594599.1:c.74A=	ENSP00000469894.1:p.Lys25=
ENST00000596375.1:c.*151A=	ENSP00000470465.1:n.*151A=
ENST00000598785.5:c.488A=	ENSP00000471830.1:p.Lys163=
ENST00000599062.5:c.581A=	ENSP00000469983.1:p.Lys194=
ENST00000601799.5:c.*889A=	ENSP00000468918.1:n.*889A=
NM_001015878.1:c.590A=	NP_001015878.1:p.Lys197=
NM_001015879.1:c.533A=	NP_001015879.1:p.Lys178=
NM_003160.2:c.488A=	NP_003151.2:p.Lys163=
XR_430209.2:n.1484A=
XR_430209.3:n.1527A=
NM_001015878.2:c.590A= MANE Select	NP_001015878.1:p.Lys197=
NM_001015879.2:c.533A=	NP_001015879.1:p.Lys178=
NM_003160.3:c.488A=	NP_003151.2:p.Lys163=