Canonical Allele Identifier: CA509133415

Gene: AURKC

Linked Data

• dbSNP Id: rs2122810662
• MyVariant Identifiers: chr19:g.57746307A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234939A>C , CM000681.2:g.57234939A>C	GRCh38
NC_000019.9:g.57746307A>C , CM000681.1:g.57746307A>C	GRCh37
NC_000019.8:g.62438119A>C	NCBI36
NG_012134.1:g.8931A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.640A>C MANE Select	ENSP00000302898.6:p.Arg214=
ENST00000302804.11:c.640A>C	ENSP00000302898.6:p.Arg214=
ENST00000415300.6:c.583A>C	ENSP00000407162.1:p.Arg195=
ENST00000448930.5:c.535A>C	ENSP00000406798.2:p.Arg179=
ENST00000594599.1:c.124A>C	ENSP00000469894.1:p.Arg42=
ENST00000596375.1:c.*201A>C	ENSP00000470465.1:n.*201A>C
ENST00000598785.5:c.538A>C	ENSP00000471830.1:p.Arg180=
ENST00000599062.5:c.631A>C	ENSP00000469983.1:p.Arg211=
ENST00000601799.5:c.*939A>C	ENSP00000468918.1:n.*939A>C
NM_001015878.1:c.640A>C	NP_001015878.1:p.Arg214=
NM_001015879.1:c.583A>C	NP_001015879.1:p.Arg195=
NM_003160.2:c.538A>C	NP_003151.2:p.Arg180=
XR_430209.2:n.1534A>C
XR_430209.3:n.1577A>C
NM_001015878.2:c.640A>C MANE Select	NP_001015878.1:p.Arg214=
NM_001015879.2:c.583A>C	NP_001015879.1:p.Arg195=
NM_003160.3:c.538A>C	NP_003151.2:p.Arg180=