Canonical Allele Identifier: CA2344338785

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234980G= , CM000681.2:g.57234980G=	GRCh38
NC_000019.9:g.57746348G= , CM000681.1:g.57746348G=	GRCh37
NC_000019.8:g.62438160G=	NCBI36
NG_012134.1:g.8972G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.681G= MANE Select	ENSP00000302898.6:p.Val227=
ENST00000302804.11:c.681G=	ENSP00000302898.6:p.Val227=
ENST00000415300.6:c.624G=	ENSP00000407162.1:p.Val208=
ENST00000448930.5:c.576G=	ENSP00000406798.2:p.Val192=
ENST00000594599.1:c.165G=	ENSP00000469894.1:p.Val55=
ENST00000596375.1:c.*242G=	ENSP00000470465.1:n.*242G=
ENST00000598785.5:c.579G=	ENSP00000471830.1:p.Val193=
ENST00000599062.5:c.672G=	ENSP00000469983.1:p.Val224=
ENST00000601799.5:c.*980G=	ENSP00000468918.1:n.*980G=
NM_001015878.1:c.681G=	NP_001015878.1:p.Val227=
NM_001015879.1:c.624G=	NP_001015879.1:p.Val208=
NM_003160.2:c.579G=	NP_003151.2:p.Val193=
XR_430209.2:n.1575G=
XR_430209.3:n.1618G=
NM_001015878.2:c.681G= MANE Select	NP_001015878.1:p.Val227=
NM_001015879.2:c.624G=	NP_001015879.1:p.Val208=
NM_003160.3:c.579G=	NP_003151.2:p.Val193=