Canonical Allele Identifier: CA9695789

Gene: AURKC

Linked Data

• ClinVar Variation Id: 330224
• ClinVar RCV Id: RCV000288115
• dbSNP Id: rs11084490
• ExAC: 19:57742472 G / C
• gnomAD v2: 19-57742472-G-C
• gnomAD v3: 19-57231104-G-C
• gnomAD v4: 19-57231104-G-C
• MyVariant Identifiers: chr19:g.57742472G>C (hg19) ; chr19:g.57231104G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231104G>C , CM000681.2:g.57231104G>C	GRCh38
NC_000019.9:g.57742472G>C , CM000681.1:g.57742472G>C	GRCh37
NC_000019.8:g.62434284G>C	NCBI36
NG_012134.1:g.5096G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000302804.12:c.-145G>C MANE Select	ENSP00000302898.6:n.-145G>C
ENST00000302804.11:c.-145G>C	ENSP00000302898.6:n.-145G>C
ENST00000415300.6:c.-10G>C	ENSP00000407162.1:n.-10G>C
ENST00000448930.5:c.-61G>C	ENSP00000406798.2:n.-61G>C
NM_001015878.1:c.-145G>C	NP_001015878.1:n.-145G>C
NM_001015879.1:c.-10G>C	NP_001015879.1:n.-10G>C
NM_003160.2:c.-60G>C	NP_003151.2:n.-60G>C
XR_430209.2:n.745G>C
XR_430209.3:n.788G>C
NM_001015878.2:c.-145G>C MANE Select	NP_001015878.1:n.-145G>C
NM_001015879.2:c.-10G>C	NP_001015879.1:n.-10G>C
NM_003160.3:c.-60G>C	NP_003151.2:n.-60G>C