Canonical Allele Identifier: CA509133437

Gene: AURKC

Linked Data

• dbSNP Id: rs2087532057
• MyVariant Identifiers: chr19:g.57746354C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234986C>T , CM000681.2:g.57234986C>T	GRCh38
NC_000019.9:g.57746354C>T , CM000681.1:g.57746354C>T	GRCh37
NC_000019.8:g.62438166C>T	NCBI36
NG_012134.1:g.8978C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.687C>T MANE Select	ENSP00000302898.6:p.Cys229=
ENST00000302804.11:c.687C>T	ENSP00000302898.6:p.Cys229=
ENST00000415300.6:c.630C>T	ENSP00000407162.1:p.Cys210=
ENST00000448930.5:c.582C>T	ENSP00000406798.2:p.Cys194=
ENST00000594599.1:c.171C>T	ENSP00000469894.1:p.Cys57=
ENST00000596375.1:c.*248C>T	ENSP00000470465.1:n.*248C>T
ENST00000598785.5:c.585C>T	ENSP00000471830.1:p.Cys195=
ENST00000599062.5:c.678C>T	ENSP00000469983.1:p.Cys226=
ENST00000601799.5:c.*986C>T	ENSP00000468918.1:n.*986C>T
NM_001015878.1:c.687C>T	NP_001015878.1:p.Cys229=
NM_001015879.1:c.630C>T	NP_001015879.1:p.Cys210=
NM_003160.2:c.585C>T	NP_003151.2:p.Cys195=
XR_430209.2:n.1581C>T
XR_430209.3:n.1624C>T
NM_001015878.2:c.687C>T MANE Select	NP_001015878.1:p.Cys229=
NM_001015879.2:c.630C>T	NP_001015879.1:p.Cys210=
NM_003160.3:c.585C>T	NP_003151.2:p.Cys195=