Canonical Allele Identifier: CA407692461

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746256A>C (hg19) ; chr19:g.57234888A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234888A>C , CM000681.2:g.57234888A>C	GRCh38
NC_000019.9:g.57746256A>C , CM000681.1:g.57746256A>C	GRCh37
NC_000019.8:g.62438068A>C	NCBI36
NG_012134.1:g.8880A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.589A>C MANE Select	ENSP00000302898.6:p.Lys197Gln
ENST00000302804.11:c.589A>C	ENSP00000302898.6:p.Lys197Gln
ENST00000415300.6:c.532A>C	ENSP00000407162.1:p.Lys178Gln
ENST00000448930.5:c.484A>C	ENSP00000406798.2:p.Lys162Gln
ENST00000594599.1:c.73A>C	ENSP00000469894.1:p.Lys25Gln
ENST00000596375.1:c.*150A>C	ENSP00000470465.1:n.*150A>C
ENST00000598785.5:c.487A>C	ENSP00000471830.1:p.Lys163Gln
ENST00000599062.5:c.580A>C	ENSP00000469983.1:p.Lys194Gln
ENST00000601799.5:c.*888A>C	ENSP00000468918.1:n.*888A>C
NM_001015878.1:c.589A>C	NP_001015878.1:p.Lys197Gln
NM_001015879.1:c.532A>C	NP_001015879.1:p.Lys178Gln
NM_003160.2:c.487A>C	NP_003151.2:p.Lys163Gln
XR_430209.2:n.1483A>C
XR_430209.3:n.1526A>C
NM_001015878.2:c.589A>C MANE Select	NP_001015878.1:p.Lys197Gln
NM_001015879.2:c.532A>C	NP_001015879.1:p.Lys178Gln
NM_003160.3:c.487A>C	NP_003151.2:p.Lys163Gln