Canonical Allele Identifier: CA407693017

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746337T>C (hg19) ; chr19:g.57234969T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234969T>C , CM000681.2:g.57234969T>C	GRCh38
NC_000019.9:g.57746337T>C , CM000681.1:g.57746337T>C	GRCh37
NC_000019.8:g.62438149T>C	NCBI36
NG_012134.1:g.8961T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.670T>C MANE Select	ENSP00000302898.6:p.Cys224Arg
ENST00000302804.11:c.670T>C	ENSP00000302898.6:p.Cys224Arg
ENST00000415300.6:c.613T>C	ENSP00000407162.1:p.Cys205Arg
ENST00000448930.5:c.565T>C	ENSP00000406798.2:p.Cys189Arg
ENST00000594599.1:c.154T>C	ENSP00000469894.1:p.Cys52Arg
ENST00000596375.1:c.*231T>C	ENSP00000470465.1:n.*231T>C
ENST00000598785.5:c.568T>C	ENSP00000471830.1:p.Cys190Arg
ENST00000599062.5:c.661T>C	ENSP00000469983.1:p.Cys221Arg
ENST00000601799.5:c.*969T>C	ENSP00000468918.1:n.*969T>C
NM_001015878.1:c.670T>C	NP_001015878.1:p.Cys224Arg
NM_001015879.1:c.613T>C	NP_001015879.1:p.Cys205Arg
NM_003160.2:c.568T>C	NP_003151.2:p.Cys190Arg
XR_430209.2:n.1564T>C
XR_430209.3:n.1607T>C
NM_001015878.2:c.670T>C MANE Select	NP_001015878.1:p.Cys224Arg
NM_001015879.2:c.613T>C	NP_001015879.1:p.Cys205Arg
NM_003160.3:c.568T>C	NP_003151.2:p.Cys190Arg