Canonical Allele Identifier: CA16576007

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57233767A>C , CM000681.2:g.57233767A>C	GRCh38
NC_000019.9:g.57745135A>C , CM000681.1:g.57745135A>C	GRCh37
NC_000019.8:g.62436947A>C	NCBI36
NG_012134.1:g.7759A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.584+159A>C MANE Select	ENSP00000302898.6:n.584+159A>C
ENST00000302804.11:c.584+159A>C	ENSP00000302898.6:n.584+159A>C
ENST00000415300.6:c.527+159A>C	ENSP00000407162.1:n.527+159A>C
ENST00000448930.5:c.480+159A>C	ENSP00000406798.2:n.480+159A>C
ENST00000594599.1:c.68+1082A>C	ENSP00000469894.1:n.68+1082A>C
ENST00000596375.1:c.*145+159A>C	ENSP00000470465.1:n.*145+159A>C
ENST00000598785.5:c.482+159A>C	ENSP00000471830.1:n.482+159A>C
ENST00000599062.5:c.575+159A>C	ENSP00000469983.1:n.575+159A>C
ENST00000601799.5:c.*883+159A>C	ENSP00000468918.1:n.*883+159A>C
NM_001015878.1:c.584+159A>C	NP_001015878.1:n.584+159A>C
NM_001015879.1:c.527+159A>C	NP_001015879.1:n.527+159A>C
NM_003160.2:c.482+159A>C	NP_003151.2:n.482+159A>C
XR_430209.2:n.1478+159A>C
XR_430209.3:n.1521+159A>C
NM_001015878.2:c.584+159A>C MANE Select	NP_001015878.1:n.584+159A>C
NM_001015879.2:c.527+159A>C	NP_001015879.1:n.527+159A>C
NM_003160.3:c.482+159A>C	NP_003151.2:n.482+159A>C