Canonical Allele Identifier: CA407692449

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746254G>C (hg19) ; chr19:g.57234886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234886G>C , CM000681.2:g.57234886G>C	GRCh38
NC_000019.9:g.57746254G>C , CM000681.1:g.57746254G>C	GRCh37
NC_000019.8:g.62438066G>C	NCBI36
NG_012134.1:g.8878G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.587G>C MANE Select	ENSP00000302898.6:p.Arg196Thr
ENST00000302804.11:c.587G>C	ENSP00000302898.6:p.Arg196Thr
ENST00000415300.6:c.530G>C	ENSP00000407162.1:p.Arg177Thr
ENST00000448930.5:c.482G>C	ENSP00000406798.2:p.Arg161Thr
ENST00000594599.1:c.71G>C	ENSP00000469894.1:p.Arg24Thr
ENST00000596375.1:c.*148G>C	ENSP00000470465.1:n.*148G>C
ENST00000598785.5:c.485G>C	ENSP00000471830.1:p.Arg162Thr
ENST00000599062.5:c.578G>C	ENSP00000469983.1:p.Arg193Thr
ENST00000601799.5:c.*886G>C	ENSP00000468918.1:n.*886G>C
NM_001015878.1:c.587G>C	NP_001015878.1:p.Arg196Thr
NM_001015879.1:c.530G>C	NP_001015879.1:p.Arg177Thr
NM_003160.2:c.485G>C	NP_003151.2:p.Arg162Thr
XR_430209.2:n.1481G>C
XR_430209.3:n.1524G>C
NM_001015878.2:c.587G>C MANE Select	NP_001015878.1:p.Arg196Thr
NM_001015879.2:c.530G>C	NP_001015879.1:p.Arg177Thr
NM_003160.3:c.485G>C	NP_003151.2:p.Arg162Thr