Canonical Allele Identifier: CA407692865

Gene: AURKC

Linked Data

• dbSNP Id: rs2087531306
• MyVariant Identifiers: chr19:g.57746308G>A (hg19) ; chr19:g.57234940G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234940G>A , CM000681.2:g.57234940G>A	GRCh38
NC_000019.9:g.57746308G>A , CM000681.1:g.57746308G>A	GRCh37
NC_000019.8:g.62438120G>A	NCBI36
NG_012134.1:g.8932G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.641G>A MANE Select	ENSP00000302898.6:p.Arg214Lys
ENST00000302804.11:c.641G>A	ENSP00000302898.6:p.Arg214Lys
ENST00000415300.6:c.584G>A	ENSP00000407162.1:p.Arg195Lys
ENST00000448930.5:c.536G>A	ENSP00000406798.2:p.Arg179Lys
ENST00000594599.1:c.125G>A	ENSP00000469894.1:p.Arg42Lys
ENST00000596375.1:c.*202G>A	ENSP00000470465.1:n.*202G>A
ENST00000598785.5:c.539G>A	ENSP00000471830.1:p.Arg180Lys
ENST00000599062.5:c.632G>A	ENSP00000469983.1:p.Arg211Lys
ENST00000601799.5:c.*940G>A	ENSP00000468918.1:n.*940G>A
NM_001015878.1:c.641G>A	NP_001015878.1:p.Arg214Lys
NM_001015879.1:c.584G>A	NP_001015879.1:p.Arg195Lys
NM_003160.2:c.539G>A	NP_003151.2:p.Arg180Lys
XR_430209.2:n.1535G>A
XR_430209.3:n.1578G>A
NM_001015878.2:c.641G>A MANE Select	NP_001015878.1:p.Arg214Lys
NM_001015879.2:c.584G>A	NP_001015879.1:p.Arg195Lys
NM_003160.3:c.539G>A	NP_003151.2:p.Arg180Lys