Canonical Allele Identifier: CA509133409

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746300T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234932T>C , CM000681.2:g.57234932T>C	GRCh38
NC_000019.9:g.57746300T>C , CM000681.1:g.57746300T>C	GRCh37
NC_000019.8:g.62438112T>C	NCBI36
NG_012134.1:g.8924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.633T>C MANE Select	ENSP00000302898.6:p.Ile211=
ENST00000302804.11:c.633T>C	ENSP00000302898.6:p.Ile211=
ENST00000415300.6:c.576T>C	ENSP00000407162.1:p.Ile192=
ENST00000448930.5:c.528T>C	ENSP00000406798.2:p.Ile176=
ENST00000594599.1:c.117T>C	ENSP00000469894.1:p.Ile39=
ENST00000596375.1:c.*194T>C	ENSP00000470465.1:n.*194T>C
ENST00000598785.5:c.531T>C	ENSP00000471830.1:p.Ile177=
ENST00000599062.5:c.624T>C	ENSP00000469983.1:p.Ile208=
ENST00000601799.5:c.*932T>C	ENSP00000468918.1:n.*932T>C
NM_001015878.1:c.633T>C	NP_001015878.1:p.Ile211=
NM_001015879.1:c.576T>C	NP_001015879.1:p.Ile192=
NM_003160.2:c.531T>C	NP_003151.2:p.Ile177=
XR_430209.2:n.1527T>C
XR_430209.3:n.1570T>C
NM_001015878.2:c.633T>C MANE Select	NP_001015878.1:p.Ile211=
NM_001015879.2:c.576T>C	NP_001015879.1:p.Ile192=
NM_003160.3:c.531T>C	NP_003151.2:p.Ile177=