Canonical Allele Identifier: CA509133393

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746270G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234902G>T , CM000681.2:g.57234902G>T	GRCh38
NC_000019.9:g.57746270G>T , CM000681.1:g.57746270G>T	GRCh37
NC_000019.8:g.62438082G>T	NCBI36
NG_012134.1:g.8894G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.603G>T MANE Select	ENSP00000302898.6:p.Gly201=
ENST00000302804.11:c.603G>T	ENSP00000302898.6:p.Gly201=
ENST00000415300.6:c.546G>T	ENSP00000407162.1:p.Gly182=
ENST00000448930.5:c.498G>T	ENSP00000406798.2:p.Gly166=
ENST00000594599.1:c.87G>T	ENSP00000469894.1:p.Gly29=
ENST00000596375.1:c.*164G>T	ENSP00000470465.1:n.*164G>T
ENST00000598785.5:c.501G>T	ENSP00000471830.1:p.Gly167=
ENST00000599062.5:c.594G>T	ENSP00000469983.1:p.Gly198=
ENST00000601799.5:c.*902G>T	ENSP00000468918.1:n.*902G>T
NM_001015878.1:c.603G>T	NP_001015878.1:p.Gly201=
NM_001015879.1:c.546G>T	NP_001015879.1:p.Gly182=
NM_003160.2:c.501G>T	NP_003151.2:p.Gly167=
XR_430209.2:n.1497G>T
XR_430209.3:n.1540G>T
NM_001015878.2:c.603G>T MANE Select	NP_001015878.1:p.Gly201=
NM_001015879.2:c.546G>T	NP_001015879.1:p.Gly182=
NM_003160.3:c.501G>T	NP_003151.2:p.Gly167=