Canonical Allele Identifier: CA2344338777

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234960G= , CM000681.2:g.57234960G=	GRCh38
NC_000019.9:g.57746328G= , CM000681.1:g.57746328G=	GRCh37
NC_000019.8:g.62438140G=	NCBI36
NG_012134.1:g.8952G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.661G= MANE Select	ENSP00000302898.6:p.Asp221=
ENST00000302804.11:c.661G=	ENSP00000302898.6:p.Asp221=
ENST00000415300.6:c.604G=	ENSP00000407162.1:p.Asp202=
ENST00000448930.5:c.556G=	ENSP00000406798.2:p.Asp186=
ENST00000594599.1:c.145G=	ENSP00000469894.1:p.Asp49=
ENST00000596375.1:c.*222G=	ENSP00000470465.1:n.*222G=
ENST00000598785.5:c.559G=	ENSP00000471830.1:p.Asp187=
ENST00000599062.5:c.652G=	ENSP00000469983.1:p.Asp218=
ENST00000601799.5:c.*960G=	ENSP00000468918.1:n.*960G=
NM_001015878.1:c.661G=	NP_001015878.1:p.Asp221=
NM_001015879.1:c.604G=	NP_001015879.1:p.Asp202=
NM_003160.2:c.559G=	NP_003151.2:p.Asp187=
XR_430209.2:n.1555G=
XR_430209.3:n.1598G=
NM_001015878.2:c.661G= MANE Select	NP_001015878.1:p.Asp221=
NM_001015879.2:c.604G=	NP_001015879.1:p.Asp202=
NM_003160.3:c.559G=	NP_003151.2:p.Asp187=