Canonical Allele Identifier: CA509133388

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746261A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234893A>G , CM000681.2:g.57234893A>G	GRCh38
NC_000019.9:g.57746261A>G , CM000681.1:g.57746261A>G	GRCh37
NC_000019.8:g.62438073A>G	NCBI36
NG_012134.1:g.8885A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.594A>G MANE Select	ENSP00000302898.6:p.Thr198=
ENST00000302804.11:c.594A>G	ENSP00000302898.6:p.Thr198=
ENST00000415300.6:c.537A>G	ENSP00000407162.1:p.Thr179=
ENST00000448930.5:c.489A>G	ENSP00000406798.2:p.Thr163=
ENST00000594599.1:c.78A>G	ENSP00000469894.1:p.Thr26=
ENST00000596375.1:c.*155A>G	ENSP00000470465.1:n.*155A>G
ENST00000598785.5:c.492A>G	ENSP00000471830.1:p.Thr164=
ENST00000599062.5:c.585A>G	ENSP00000469983.1:p.Thr195=
ENST00000601799.5:c.*893A>G	ENSP00000468918.1:n.*893A>G
NM_001015878.1:c.594A>G	NP_001015878.1:p.Thr198=
NM_001015879.1:c.537A>G	NP_001015879.1:p.Thr179=
NM_003160.2:c.492A>G	NP_003151.2:p.Thr164=
XR_430209.2:n.1488A>G
XR_430209.3:n.1531A>G
NM_001015878.2:c.594A>G MANE Select	NP_001015878.1:p.Thr198=
NM_001015879.2:c.537A>G	NP_001015879.1:p.Thr179=
NM_003160.3:c.492A>G	NP_003151.2:p.Thr164=