Canonical Allele Identifier: CA310426735

Gene: AURKC

Linked Data

• dbSNP Id: rs200042694
• gnomAD v3: 19-57234890-G-T
• gnomAD v4: 19-57234890-G-T
• MyVariant Identifiers: chr19:g.57746258G>T (hg19) ; chr19:g.57234890G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234890G>T , CM000681.2:g.57234890G>T	GRCh38
NC_000019.9:g.57746258G>T , CM000681.1:g.57746258G>T	GRCh37
NC_000019.8:g.62438070G>T	NCBI36
NG_012134.1:g.8882G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.591G>T MANE Select	ENSP00000302898.6:p.Lys197Asn
ENST00000302804.11:c.591G>T	ENSP00000302898.6:p.Lys197Asn
ENST00000415300.6:c.534G>T	ENSP00000407162.1:p.Lys178Asn
ENST00000448930.5:c.486G>T	ENSP00000406798.2:p.Lys162Asn
ENST00000594599.1:c.75G>T	ENSP00000469894.1:p.Lys25Asn
ENST00000596375.1:c.*152G>T	ENSP00000470465.1:n.*152G>T
ENST00000598785.5:c.489G>T	ENSP00000471830.1:p.Lys163Asn
ENST00000599062.5:c.582G>T	ENSP00000469983.1:p.Lys194Asn
ENST00000601799.5:c.*890G>T	ENSP00000468918.1:n.*890G>T
NM_001015878.1:c.591G>T	NP_001015878.1:p.Lys197Asn
NM_001015879.1:c.534G>T	NP_001015879.1:p.Lys178Asn
NM_003160.2:c.489G>T	NP_003151.2:p.Lys163Asn
XR_430209.2:n.1485G>T
XR_430209.3:n.1528G>T
NM_001015878.2:c.591G>T MANE Select	NP_001015878.1:p.Lys197Asn
NM_001015879.2:c.534G>T	NP_001015879.1:p.Lys178Asn
NM_003160.3:c.489G>T	NP_003151.2:p.Lys163Asn