Canonical Allele Identifier: CA407692508

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746260C>G (hg19) ; chr19:g.57234892C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234892C>G , CM000681.2:g.57234892C>G	GRCh38
NC_000019.9:g.57746260C>G , CM000681.1:g.57746260C>G	GRCh37
NC_000019.8:g.62438072C>G	NCBI36
NG_012134.1:g.8884C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.593C>G MANE Select	ENSP00000302898.6:p.Thr198Arg
ENST00000302804.11:c.593C>G	ENSP00000302898.6:p.Thr198Arg
ENST00000415300.6:c.536C>G	ENSP00000407162.1:p.Thr179Arg
ENST00000448930.5:c.488C>G	ENSP00000406798.2:p.Thr163Arg
ENST00000594599.1:c.77C>G	ENSP00000469894.1:p.Thr26Arg
ENST00000596375.1:c.*154C>G	ENSP00000470465.1:n.*154C>G
ENST00000598785.5:c.491C>G	ENSP00000471830.1:p.Thr164Arg
ENST00000599062.5:c.584C>G	ENSP00000469983.1:p.Thr195Arg
ENST00000601799.5:c.*892C>G	ENSP00000468918.1:n.*892C>G
NM_001015878.1:c.593C>G	NP_001015878.1:p.Thr198Arg
NM_001015879.1:c.536C>G	NP_001015879.1:p.Thr179Arg
NM_003160.2:c.491C>G	NP_003151.2:p.Thr164Arg
XR_430209.2:n.1487C>G
XR_430209.3:n.1530C>G
NM_001015878.2:c.593C>G MANE Select	NP_001015878.1:p.Thr198Arg
NM_001015879.2:c.536C>G	NP_001015879.1:p.Thr179Arg
NM_003160.3:c.491C>G	NP_003151.2:p.Thr164Arg