Canonical Allele Identifier: CA407692888

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746311C>G (hg19) ; chr19:g.57234943C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234943C>G , CM000681.2:g.57234943C>G	GRCh38
NC_000019.9:g.57746311C>G , CM000681.1:g.57746311C>G	GRCh37
NC_000019.8:g.62438123C>G	NCBI36
NG_012134.1:g.8935C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.644C>G MANE Select	ENSP00000302898.6:p.Thr215Arg
ENST00000302804.11:c.644C>G	ENSP00000302898.6:p.Thr215Arg
ENST00000415300.6:c.587C>G	ENSP00000407162.1:p.Thr196Arg
ENST00000448930.5:c.539C>G	ENSP00000406798.2:p.Thr180Arg
ENST00000594599.1:c.128C>G	ENSP00000469894.1:p.Thr43Arg
ENST00000596375.1:c.*205C>G	ENSP00000470465.1:n.*205C>G
ENST00000598785.5:c.542C>G	ENSP00000471830.1:p.Thr181Arg
ENST00000599062.5:c.635C>G	ENSP00000469983.1:p.Thr212Arg
ENST00000601799.5:c.*943C>G	ENSP00000468918.1:n.*943C>G
NM_001015878.1:c.644C>G	NP_001015878.1:p.Thr215Arg
NM_001015879.1:c.587C>G	NP_001015879.1:p.Thr196Arg
NM_003160.2:c.542C>G	NP_003151.2:p.Thr181Arg
XR_430209.2:n.1538C>G
XR_430209.3:n.1581C>G
NM_001015878.2:c.644C>G MANE Select	NP_001015878.1:p.Thr215Arg
NM_001015879.2:c.587C>G	NP_001015879.1:p.Thr196Arg
NM_003160.3:c.542C>G	NP_003151.2:p.Thr181Arg