Canonical Allele Identifier: CA2582292700
Gene: AURKC HGNC NCBI

Linked Data

dbSNP Id: rs2122798738

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.57231107A>C , CM000681.2:g.57231107A>C GRCh38
NC_000019.9:g.57742475A>C , CM000681.1:g.57742475A>C GRCh37
NC_000019.8:g.62434287A>C NCBI36
NG_012134.1:g.5099A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302804.12:c.-142A>C MANE Select ENSP00000302898.6:n.-142A>C
ENST00000302804.11:c.-142A>C ENSP00000302898.6:n.-142A>C
ENST00000415300.6:c.-7A>C ENSP00000407162.1:n.-7A>C
ENST00000448930.5:c.-58A>C ENSP00000406798.2:n.-58A>C
NM_001015878.1:c.-142A>C NP_001015878.1:n.-142A>C
NM_001015879.1:c.-7A>C NP_001015879.1:n.-7A>C
NM_003160.2:c.-57A>C NP_003151.2:n.-57A>C
XR_430209.2:n.748A>C
XR_430209.3:n.791A>C
NM_001015878.2:c.-142A>C MANE Select NP_001015878.1:n.-142A>C
NM_001015879.2:c.-7A>C NP_001015879.1:n.-7A>C
NM_003160.3:c.-57A>C NP_003151.2:n.-57A>C