Canonical Allele Identifier: CA509133413

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746306G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234938G>C , CM000681.2:g.57234938G>C	GRCh38
NC_000019.9:g.57746306G>C , CM000681.1:g.57746306G>C	GRCh37
NC_000019.8:g.62438118G>C	NCBI36
NG_012134.1:g.8930G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.639G>C MANE Select	ENSP00000302898.6:p.Gly213=
ENST00000302804.11:c.639G>C	ENSP00000302898.6:p.Gly213=
ENST00000415300.6:c.582G>C	ENSP00000407162.1:p.Gly194=
ENST00000448930.5:c.534G>C	ENSP00000406798.2:p.Gly178=
ENST00000594599.1:c.123G>C	ENSP00000469894.1:p.Gly41=
ENST00000596375.1:c.*200G>C	ENSP00000470465.1:n.*200G>C
ENST00000598785.5:c.537G>C	ENSP00000471830.1:p.Gly179=
ENST00000599062.5:c.630G>C	ENSP00000469983.1:p.Gly210=
ENST00000601799.5:c.*938G>C	ENSP00000468918.1:n.*938G>C
NM_001015878.1:c.639G>C	NP_001015878.1:p.Gly213=
NM_001015879.1:c.582G>C	NP_001015879.1:p.Gly194=
NM_003160.2:c.537G>C	NP_003151.2:p.Gly179=
XR_430209.2:n.1533G>C
XR_430209.3:n.1576G>C
NM_001015878.2:c.639G>C MANE Select	NP_001015878.1:p.Gly213=
NM_001015879.2:c.582G>C	NP_001015879.1:p.Gly194=
NM_003160.3:c.537G>C	NP_003151.2:p.Gly179=