Canonical Allele Identifier: CA2344338781

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234972A= , CM000681.2:g.57234972A=	GRCh38
NC_000019.9:g.57746340A= , CM000681.1:g.57746340A=	GRCh37
NC_000019.8:g.62438152A=	NCBI36
NG_012134.1:g.8964A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.673A= MANE Select	ENSP00000302898.6:p.Ile225=
ENST00000302804.11:c.673A=	ENSP00000302898.6:p.Ile225=
ENST00000415300.6:c.616A=	ENSP00000407162.1:p.Ile206=
ENST00000448930.5:c.568A=	ENSP00000406798.2:p.Ile190=
ENST00000594599.1:c.157A=	ENSP00000469894.1:p.Ile53=
ENST00000596375.1:c.*234A=	ENSP00000470465.1:n.*234A=
ENST00000598785.5:c.571A=	ENSP00000471830.1:p.Ile191=
ENST00000599062.5:c.664A=	ENSP00000469983.1:p.Ile222=
ENST00000601799.5:c.*972A=	ENSP00000468918.1:n.*972A=
NM_001015878.1:c.673A=	NP_001015878.1:p.Ile225=
NM_001015879.1:c.616A=	NP_001015879.1:p.Ile206=
NM_003160.2:c.571A=	NP_003151.2:p.Ile191=
XR_430209.2:n.1567A=
XR_430209.3:n.1610A=
NM_001015878.2:c.673A= MANE Select	NP_001015878.1:p.Ile225=
NM_001015879.2:c.616A=	NP_001015879.1:p.Ile206=
NM_003160.3:c.571A=	NP_003151.2:p.Ile191=