Canonical Allele Identifier: CA2587522786

Gene: AURKC

Linked Data

• gnomAD v4: 19-57231111-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231111A>C , CM000681.2:g.57231111A>C	GRCh38
NC_000019.9:g.57742479A>C , CM000681.1:g.57742479A>C	GRCh37
NC_000019.8:g.62434291A>C	NCBI36
NG_012134.1:g.5103A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-138A>C MANE Select	ENSP00000302898.6:n.-138A>C
ENST00000302804.11:c.-138A>C	ENSP00000302898.6:n.-138A>C
ENST00000415300.6:c.-3A>C	ENSP00000407162.1:n.-3A>C
ENST00000448930.5:c.-54A>C	ENSP00000406798.2:n.-54A>C
NM_001015878.1:c.-138A>C	NP_001015878.1:n.-138A>C
NM_001015879.1:c.-3A>C	NP_001015879.1:n.-3A>C
NM_003160.2:c.-53A>C	NP_003151.2:n.-53A>C
XR_430209.2:n.752A>C
XR_430209.3:n.795A>C
NM_001015878.2:c.-138A>C MANE Select	NP_001015878.1:n.-138A>C
NM_001015879.2:c.-3A>C	NP_001015879.1:n.-3A>C
NM_003160.3:c.-53A>C	NP_003151.2:n.-53A>C