Canonical Allele Identifier: CA2587522784

Gene: AURKC

Linked Data

• gnomAD v4: 19-57231109-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231109A>C , CM000681.2:g.57231109A>C	GRCh38
NC_000019.9:g.57742477A>C , CM000681.1:g.57742477A>C	GRCh37
NC_000019.8:g.62434289A>C	NCBI36
NG_012134.1:g.5101A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-140A>C MANE Select	ENSP00000302898.6:n.-140A>C
ENST00000302804.11:c.-140A>C	ENSP00000302898.6:n.-140A>C
ENST00000415300.6:c.-5A>C	ENSP00000407162.1:n.-5A>C
ENST00000448930.5:c.-56A>C	ENSP00000406798.2:n.-56A>C
NM_001015878.1:c.-140A>C	NP_001015878.1:n.-140A>C
NM_001015879.1:c.-5A>C	NP_001015879.1:n.-5A>C
NM_003160.2:c.-55A>C	NP_003151.2:n.-55A>C
XR_430209.2:n.750A>C
XR_430209.3:n.793A>C
NM_001015878.2:c.-140A>C MANE Select	NP_001015878.1:n.-140A>C
NM_001015879.2:c.-5A>C	NP_001015879.1:n.-5A>C
NM_003160.3:c.-55A>C	NP_003151.2:n.-55A>C