Canonical Allele Identifier: CA509133418

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746312A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234944A>T , CM000681.2:g.57234944A>T	GRCh38
NC_000019.9:g.57746312A>T , CM000681.1:g.57746312A>T	GRCh37
NC_000019.8:g.62438124A>T	NCBI36
NG_012134.1:g.8936A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.645A>T MANE Select	ENSP00000302898.6:p.Thr215=
ENST00000302804.11:c.645A>T	ENSP00000302898.6:p.Thr215=
ENST00000415300.6:c.588A>T	ENSP00000407162.1:p.Thr196=
ENST00000448930.5:c.540A>T	ENSP00000406798.2:p.Thr180=
ENST00000594599.1:c.129A>T	ENSP00000469894.1:p.Thr43=
ENST00000596375.1:c.*206A>T	ENSP00000470465.1:n.*206A>T
ENST00000598785.5:c.543A>T	ENSP00000471830.1:p.Thr181=
ENST00000599062.5:c.636A>T	ENSP00000469983.1:p.Thr212=
ENST00000601799.5:c.*944A>T	ENSP00000468918.1:n.*944A>T
NM_001015878.1:c.645A>T	NP_001015878.1:p.Thr215=
NM_001015879.1:c.588A>T	NP_001015879.1:p.Thr196=
NM_003160.2:c.543A>T	NP_003151.2:p.Thr181=
XR_430209.2:n.1539A>T
XR_430209.3:n.1582A>T
NM_001015878.2:c.645A>T MANE Select	NP_001015878.1:p.Thr215=
NM_001015879.2:c.588A>T	NP_001015879.1:p.Thr196=
NM_003160.3:c.543A>T	NP_003151.2:p.Thr181=