Canonical Allele Identifier: CA2344338786

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234982T= , CM000681.2:g.57234982T=	GRCh38
NC_000019.9:g.57746350T= , CM000681.1:g.57746350T=	GRCh37
NC_000019.8:g.62438162T=	NCBI36
NG_012134.1:g.8974T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.683T= MANE Select	ENSP00000302898.6:p.Leu228=
ENST00000302804.11:c.683T=	ENSP00000302898.6:p.Leu228=
ENST00000415300.6:c.626T=	ENSP00000407162.1:p.Leu209=
ENST00000448930.5:c.578T=	ENSP00000406798.2:p.Leu193=
ENST00000594599.1:c.167T=	ENSP00000469894.1:p.Leu56=
ENST00000596375.1:c.*244T=	ENSP00000470465.1:n.*244T=
ENST00000598785.5:c.581T=	ENSP00000471830.1:p.Leu194=
ENST00000599062.5:c.674T=	ENSP00000469983.1:p.Leu225=
ENST00000601799.5:c.*982T=	ENSP00000468918.1:n.*982T=
NM_001015878.1:c.683T=	NP_001015878.1:p.Leu228=
NM_001015879.1:c.626T=	NP_001015879.1:p.Leu209=
NM_003160.2:c.581T=	NP_003151.2:p.Leu194=
XR_430209.2:n.1577T=
XR_430209.3:n.1620T=
NM_001015878.2:c.683T= MANE Select	NP_001015878.1:p.Leu228=
NM_001015879.2:c.626T=	NP_001015879.1:p.Leu209=
NM_003160.3:c.581T=	NP_003151.2:p.Leu194=