Canonical Allele Identifier: CA509133399

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746276G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234908G>T , CM000681.2:g.57234908G>T	GRCh38
NC_000019.9:g.57746276G>T , CM000681.1:g.57746276G>T	GRCh37
NC_000019.8:g.62438088G>T	NCBI36
NG_012134.1:g.8900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.609G>T MANE Select	ENSP00000302898.6:p.Leu203=
ENST00000302804.11:c.609G>T	ENSP00000302898.6:p.Leu203=
ENST00000415300.6:c.552G>T	ENSP00000407162.1:p.Leu184=
ENST00000448930.5:c.504G>T	ENSP00000406798.2:p.Leu168=
ENST00000594599.1:c.93G>T	ENSP00000469894.1:p.Leu31=
ENST00000596375.1:c.*170G>T	ENSP00000470465.1:n.*170G>T
ENST00000598785.5:c.507G>T	ENSP00000471830.1:p.Leu169=
ENST00000599062.5:c.600G>T	ENSP00000469983.1:p.Leu200=
ENST00000601799.5:c.*908G>T	ENSP00000468918.1:n.*908G>T
NM_001015878.1:c.609G>T	NP_001015878.1:p.Leu203=
NM_001015879.1:c.552G>T	NP_001015879.1:p.Leu184=
NM_003160.2:c.507G>T	NP_003151.2:p.Leu169=
XR_430209.2:n.1503G>T
XR_430209.3:n.1546G>T
NM_001015878.2:c.609G>T MANE Select	NP_001015878.1:p.Leu203=
NM_001015879.2:c.552G>T	NP_001015879.1:p.Leu184=
NM_003160.3:c.507G>T	NP_003151.2:p.Leu169=