Canonical Allele Identifier: CA407692798

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746298A>C (hg19) ; chr19:g.57234930A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234930A>C , CM000681.2:g.57234930A>C	GRCh38
NC_000019.9:g.57746298A>C , CM000681.1:g.57746298A>C	GRCh37
NC_000019.8:g.62438110A>C	NCBI36
NG_012134.1:g.8922A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.631A>C MANE Select	ENSP00000302898.6:p.Ile211Leu
ENST00000302804.11:c.631A>C	ENSP00000302898.6:p.Ile211Leu
ENST00000415300.6:c.574A>C	ENSP00000407162.1:p.Ile192Leu
ENST00000448930.5:c.526A>C	ENSP00000406798.2:p.Ile176Leu
ENST00000594599.1:c.115A>C	ENSP00000469894.1:p.Ile39Leu
ENST00000596375.1:c.*192A>C	ENSP00000470465.1:n.*192A>C
ENST00000598785.5:c.529A>C	ENSP00000471830.1:p.Ile177Leu
ENST00000599062.5:c.622A>C	ENSP00000469983.1:p.Ile208Leu
ENST00000601799.5:c.*930A>C	ENSP00000468918.1:n.*930A>C
NM_001015878.1:c.631A>C	NP_001015878.1:p.Ile211Leu
NM_001015879.1:c.574A>C	NP_001015879.1:p.Ile192Leu
NM_003160.2:c.529A>C	NP_003151.2:p.Ile177Leu
XR_430209.2:n.1525A>C
XR_430209.3:n.1568A>C
NM_001015878.2:c.631A>C MANE Select	NP_001015878.1:p.Ile211Leu
NM_001015879.2:c.574A>C	NP_001015879.1:p.Ile192Leu
NM_003160.3:c.529A>C	NP_003151.2:p.Ile177Leu