Canonical Allele Identifier: CA310426738

Gene: AURKC

Linked Data

• dbSNP Id: rs937634821
• MyVariant Identifiers: chr19:g.57746266G>A (hg19) ; chr19:g.57234898G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234898G>A , CM000681.2:g.57234898G>A	GRCh38
NC_000019.9:g.57746266G>A , CM000681.1:g.57746266G>A	GRCh37
NC_000019.8:g.62438078G>A	NCBI36
NG_012134.1:g.8890G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.599G>A MANE Select	ENSP00000302898.6:p.Cys200Tyr
ENST00000302804.11:c.599G>A	ENSP00000302898.6:p.Cys200Tyr
ENST00000415300.6:c.542G>A	ENSP00000407162.1:p.Cys181Tyr
ENST00000448930.5:c.494G>A	ENSP00000406798.2:p.Cys165Tyr
ENST00000594599.1:c.83G>A	ENSP00000469894.1:p.Cys28Tyr
ENST00000596375.1:c.*160G>A	ENSP00000470465.1:n.*160G>A
ENST00000598785.5:c.497G>A	ENSP00000471830.1:p.Cys166Tyr
ENST00000599062.5:c.590G>A	ENSP00000469983.1:p.Cys197Tyr
ENST00000601799.5:c.*898G>A	ENSP00000468918.1:n.*898G>A
NM_001015878.1:c.599G>A	NP_001015878.1:p.Cys200Tyr
NM_001015879.1:c.542G>A	NP_001015879.1:p.Cys181Tyr
NM_003160.2:c.497G>A	NP_003151.2:p.Cys166Tyr
XR_430209.2:n.1493G>A
XR_430209.3:n.1536G>A
NM_001015878.2:c.599G>A MANE Select	NP_001015878.1:p.Cys200Tyr
NM_001015879.2:c.542G>A	NP_001015879.1:p.Cys181Tyr
NM_003160.3:c.497G>A	NP_003151.2:p.Cys166Tyr