Canonical Allele Identifier: CA2371346824

Gene: AURKA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56391298_56391300delinsGAA , CM000682.2:g.56391298_56391300delinsGAA	GRCh38
NC_000020.10:g.54966354_54966356delinsGAA , CM000682.1:g.54966354_54966356delinsGAA	GRCh37
NC_000020.9:g.54399761_54399763delinsGAA	NCBI36
NG_012133.1:g.5996_5998delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395915.8:c.-6+868_-6+870delinsTTC MANE Select	ENSP00000379251.3:n.-6+868_-6+870delinsTTC
ENST00000312783.10:c.-115-635_-115-633delinsTTC	ENSP00000321591.6:n.-115-635_-115-633delinsTTC
ENST00000347343.6:c.-6+643_-6+645delinsTTC	ENSP00000216911.2:n.-6+643_-6+645delinsTTC
ENST00000371356.6:c.-104+868_-104+870delinsTTC	ENSP00000360407.2:n.-104+868_-104+870delinsTTC
ENST00000395907.5:c.-6+868_-6+870delinsTTC	ENSP00000379243.1:n.-6+868_-6+870delinsTTC
ENST00000395911.5:c.-104+854_-104+856delinsTTC	ENSP00000379247.1:n.-104+854_-104+856delinsTTC
ENST00000395913.7:c.-6+854_-6+856delinsTTC	ENSP00000379249.3:n.-6+854_-6+856delinsTTC
ENST00000395914.5:c.-115-635_-115-633delinsTTC	ENSP00000379250.1:n.-115-635_-115-633delinsTTC
ENST00000395915.7:c.-6+868_-6+870delinsTTC	ENSP00000379251.3:n.-6+868_-6+870delinsTTC
ENST00000420474.5:c.-213-635_-213-633delinsTTC	ENSP00000388073.1:n.-213-635_-213-633delinsTTC
ENST00000422322.5:c.-115-635_-115-633delinsTTC	ENSP00000405042.1:n.-115-635_-115-633delinsTTC
ENST00000441357.5:c.-115-635_-115-633delinsTTC	ENSP00000393452.1:n.-115-635_-115-633delinsTTC
ENST00000451915.1:c.-310-635_-310-633delinsTTC	ENSP00000401358.1:n.-310-635_-310-633delinsTTC
ENST00000456249.5:c.-213-635_-213-633delinsTTC	ENSP00000405170.1:n.-213-635_-213-633delinsTTC
NM_003600.2:c.-6+643_-6+645delinsTTC	NP_003591.2:n.-6+643_-6+645delinsTTC
NM_198433.1:c.-213-635_-213-633delinsTTC	NP_940835.1:n.-213-635_-213-633delinsTTC
NM_198434.1:c.-115-635_-115-633delinsTTC	NP_940836.1:n.-115-635_-115-633delinsTTC
NM_198435.1:c.-6+854_-6+856delinsTTC	NP_940837.1:n.-6+854_-6+856delinsTTC
NM_198436.1:c.-115-635_-115-633delinsTTC	NP_940838.1:n.-115-635_-115-633delinsTTC
NM_198437.1:c.-6+868_-6+870delinsTTC	NP_940839.1:n.-6+868_-6+870delinsTTC
XM_005260534.1:c.-115-635_-115-633delinsTTC	XP_005260591.1:n.-115-635_-115-633delinsTTC
XM_006723872.1:c.-104+643_-104+645delinsTTC	XP_006723935.1:n.-104+643_-104+645delinsTTC
NM_001323303.1:c.-115-635_-115-633delinsTTC	NP_001310232.1:n.-115-635_-115-633delinsTTC
NM_001323304.1:c.-104+868_-104+870delinsTTC	NP_001310233.1:n.-104+868_-104+870delinsTTC
NM_001323305.1:c.-213-635_-213-633delinsTTC	NP_001310234.1:n.-213-635_-213-633delinsTTC
NM_003600.3:c.-6+643_-6+645delinsTTC	NP_003591.2:n.-6+643_-6+645delinsTTC
NM_198433.2:c.-213-635_-213-633delinsTTC	NP_940835.1:n.-213-635_-213-633delinsTTC
NM_198434.2:c.-115-635_-115-633delinsTTC	NP_940836.1:n.-115-635_-115-633delinsTTC
NM_198435.2:c.-6+854_-6+856delinsTTC	NP_940837.1:n.-6+854_-6+856delinsTTC
NM_198436.2:c.-115-635_-115-633delinsTTC	NP_940838.1:n.-115-635_-115-633delinsTTC
NM_198437.2:c.-6+868_-6+870delinsTTC	NP_940839.1:n.-6+868_-6+870delinsTTC
XM_017028034.2:c.-486-635_-486-633delinsTTC	XP_016883523.1:n.-486-635_-486-633delinsTTC
XM_017028035.1:c.-6+491_-6+493delinsTTC	XP_016883524.1:n.-6+491_-6+493delinsTTC
XM_024451974.1:c.-213-635_-213-633delinsTTC	XP_024307742.1:n.-213-635_-213-633delinsTTC
NM_001323303.2:c.-115-635_-115-633delinsTTC	NP_001310232.1:n.-115-635_-115-633delinsTTC
NM_001323304.2:c.-104+868_-104+870delinsTTC	NP_001310233.1:n.-104+868_-104+870delinsTTC
NM_001323305.2:c.-213-635_-213-633delinsTTC	NP_001310234.1:n.-213-635_-213-633delinsTTC
NM_003600.4:c.-6+643_-6+645delinsTTC	NP_003591.2:n.-6+643_-6+645delinsTTC
NM_198433.3:c.-213-635_-213-633delinsTTC	NP_940835.1:n.-213-635_-213-633delinsTTC
NM_198435.3:c.-6+854_-6+856delinsTTC	NP_940837.1:n.-6+854_-6+856delinsTTC
NM_198436.3:c.-115-635_-115-633delinsTTC	NP_940838.1:n.-115-635_-115-633delinsTTC
NM_198437.3:c.-6+868_-6+870delinsTTC MANE Select	NP_940839.1:n.-6+868_-6+870delinsTTC
NM_198434.3:c.-115-635_-115-633delinsTTC	NP_940836.1:n.-115-635_-115-633delinsTTC