Canonical Allele Identifier: CA2344338766

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234936G= , CM000681.2:g.57234936G=	GRCh38
NC_000019.9:g.57746304G= , CM000681.1:g.57746304G=	GRCh37
NC_000019.8:g.62438116G=	NCBI36
NG_012134.1:g.8928G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.637G= MANE Select	ENSP00000302898.6:p.Gly213=
ENST00000302804.11:c.637G=	ENSP00000302898.6:p.Gly213=
ENST00000415300.6:c.580G=	ENSP00000407162.1:p.Gly194=
ENST00000448930.5:c.532G=	ENSP00000406798.2:p.Gly178=
ENST00000594599.1:c.121G=	ENSP00000469894.1:p.Gly41=
ENST00000596375.1:c.*198G=	ENSP00000470465.1:n.*198G=
ENST00000598785.5:c.535G=	ENSP00000471830.1:p.Gly179=
ENST00000599062.5:c.628G=	ENSP00000469983.1:p.Gly210=
ENST00000601799.5:c.*936G=	ENSP00000468918.1:n.*936G=
NM_001015878.1:c.637G=	NP_001015878.1:p.Gly213=
NM_001015879.1:c.580G=	NP_001015879.1:p.Gly194=
NM_003160.2:c.535G=	NP_003151.2:p.Gly179=
XR_430209.2:n.1531G=
XR_430209.3:n.1574G=
NM_001015878.2:c.637G= MANE Select	NP_001015878.1:p.Gly213=
NM_001015879.2:c.580G=	NP_001015879.1:p.Gly194=
NM_003160.3:c.535G=	NP_003151.2:p.Gly179=