Canonical Allele Identifier: CA407692939

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746321A>C (hg19) ; chr19:g.57234953A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234953A>C , CM000681.2:g.57234953A>C	GRCh38
NC_000019.9:g.57746321A>C , CM000681.1:g.57746321A>C	GRCh37
NC_000019.8:g.62438133A>C	NCBI36
NG_012134.1:g.8945A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.654A>C MANE Select	ENSP00000302898.6:p.Glu218Asp
ENST00000302804.11:c.654A>C	ENSP00000302898.6:p.Glu218Asp
ENST00000415300.6:c.597A>C	ENSP00000407162.1:p.Glu199Asp
ENST00000448930.5:c.549A>C	ENSP00000406798.2:p.Glu183Asp
ENST00000594599.1:c.138A>C	ENSP00000469894.1:p.Glu46Asp
ENST00000596375.1:c.*215A>C	ENSP00000470465.1:n.*215A>C
ENST00000598785.5:c.552A>C	ENSP00000471830.1:p.Glu184Asp
ENST00000599062.5:c.645A>C	ENSP00000469983.1:p.Glu215Asp
ENST00000601799.5:c.*953A>C	ENSP00000468918.1:n.*953A>C
NM_001015878.1:c.654A>C	NP_001015878.1:p.Glu218Asp
NM_001015879.1:c.597A>C	NP_001015879.1:p.Glu199Asp
NM_003160.2:c.552A>C	NP_003151.2:p.Glu184Asp
XR_430209.2:n.1548A>C
XR_430209.3:n.1591A>C
NM_001015878.2:c.654A>C MANE Select	NP_001015878.1:p.Glu218Asp
NM_001015879.2:c.597A>C	NP_001015879.1:p.Glu199Asp
NM_003160.3:c.552A>C	NP_003151.2:p.Glu184Asp