Canonical Allele Identifier: CA407693095

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746354C>A (hg19) ; chr19:g.57234986C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.687C>A MANE Select	ENSP00000302898.6:p.Cys229Ter
ENST00000302804.11:c.687C>A	ENSP00000302898.6:p.Cys229Ter
ENST00000415300.6:c.630C>A	ENSP00000407162.1:p.Cys210Ter
ENST00000448930.5:c.582C>A	ENSP00000406798.2:p.Cys194Ter
ENST00000594599.1:c.171C>A	ENSP00000469894.1:p.Cys57Ter
ENST00000596375.1:c.*248C>A	ENSP00000470465.1:n.*248C>A
ENST00000598785.5:c.585C>A	ENSP00000471830.1:p.Cys195Ter
ENST00000599062.5:c.678C>A	ENSP00000469983.1:p.Cys226Ter
ENST00000601799.5:c.*986C>A	ENSP00000468918.1:n.*986C>A
NM_001015878.1:c.687C>A	NP_001015878.1:p.Cys229Ter
NM_001015879.1:c.630C>A	NP_001015879.1:p.Cys210Ter
NM_003160.2:c.585C>A	NP_003151.2:p.Cys195Ter
XR_430209.2:n.1581C>A
XR_430209.3:n.1624C>A
NM_001015878.2:c.687C>A MANE Select	NP_001015878.1:p.Cys229Ter
NM_001015879.2:c.630C>A	NP_001015879.1:p.Cys210Ter
NM_003160.3:c.585C>A	NP_003151.2:p.Cys195Ter