Canonical Allele Identifier: CA2371346828

Gene: AURKA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56391306_56391307delinsAT , CM000682.2:g.56391306_56391307delinsAT	GRCh38
NC_000020.10:g.54966362_54966363delinsAT , CM000682.1:g.54966362_54966363delinsAT	GRCh37
NC_000020.9:g.54399769_54399770delinsAT	NCBI36
NG_012133.1:g.5989_5990delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000395915.8:c.-6+861_-6+862delinsAT MANE Select	ENSP00000379251.3:n.-6+861_-6+862delinsAT
ENST00000312783.10:c.-115-642_-115-641delinsAT	ENSP00000321591.6:n.-115-642_-115-641delinsAT
ENST00000347343.6:c.-6+636_-6+637delinsAT	ENSP00000216911.2:n.-6+636_-6+637delinsAT
ENST00000371356.6:c.-104+861_-104+862delinsAT	ENSP00000360407.2:n.-104+861_-104+862delinsAT
ENST00000395907.5:c.-6+861_-6+862delinsAT	ENSP00000379243.1:n.-6+861_-6+862delinsAT
ENST00000395911.5:c.-104+847_-104+848delinsAT	ENSP00000379247.1:n.-104+847_-104+848delinsAT
ENST00000395913.7:c.-6+847_-6+848delinsAT	ENSP00000379249.3:n.-6+847_-6+848delinsAT
ENST00000395914.5:c.-115-642_-115-641delinsAT	ENSP00000379250.1:n.-115-642_-115-641delinsAT
ENST00000395915.7:c.-6+861_-6+862delinsAT	ENSP00000379251.3:n.-6+861_-6+862delinsAT
ENST00000420474.5:c.-213-642_-213-641delinsAT	ENSP00000388073.1:n.-213-642_-213-641delinsAT
ENST00000422322.5:c.-116+636_-116+637delinsAT	ENSP00000405042.1:n.-116+636_-116+637delinsAT
ENST00000441357.5:c.-115-642_-115-641delinsAT	ENSP00000393452.1:n.-115-642_-115-641delinsAT
ENST00000451915.1:c.-310-642_-310-641delinsAT	ENSP00000401358.1:n.-310-642_-310-641delinsAT
ENST00000456249.5:c.-214+636_-214+637delinsAT	ENSP00000405170.1:n.-214+636_-214+637delinsAT
NM_003600.2:c.-6+636_-6+637delinsAT	NP_003591.2:n.-6+636_-6+637delinsAT
NM_198433.1:c.-214+636_-214+637delinsAT	NP_940835.1:n.-214+636_-214+637delinsAT
NM_198434.1:c.-115-642_-115-641delinsAT	NP_940836.1:n.-115-642_-115-641delinsAT
NM_198435.1:c.-6+847_-6+848delinsAT	NP_940837.1:n.-6+847_-6+848delinsAT
NM_198436.1:c.-115-642_-115-641delinsAT	NP_940838.1:n.-115-642_-115-641delinsAT
NM_198437.1:c.-6+861_-6+862delinsAT	NP_940839.1:n.-6+861_-6+862delinsAT
XM_005260534.1:c.-116+636_-116+637delinsAT	XP_005260591.1:n.-116+636_-116+637delinsAT
XM_006723872.1:c.-104+636_-104+637delinsAT	XP_006723935.1:n.-104+636_-104+637delinsAT
NM_001323303.1:c.-116+636_-116+637delinsAT	NP_001310232.1:n.-116+636_-116+637delinsAT
NM_001323304.1:c.-104+861_-104+862delinsAT	NP_001310233.1:n.-104+861_-104+862delinsAT
NM_001323305.1:c.-213-642_-213-641delinsAT	NP_001310234.1:n.-213-642_-213-641delinsAT
NM_003600.3:c.-6+636_-6+637delinsAT	NP_003591.2:n.-6+636_-6+637delinsAT
NM_198433.2:c.-214+636_-214+637delinsAT	NP_940835.1:n.-214+636_-214+637delinsAT
NM_198434.2:c.-115-642_-115-641delinsAT	NP_940836.1:n.-115-642_-115-641delinsAT
NM_198435.2:c.-6+847_-6+848delinsAT	NP_940837.1:n.-6+847_-6+848delinsAT
NM_198436.2:c.-115-642_-115-641delinsAT	NP_940838.1:n.-115-642_-115-641delinsAT
NM_198437.2:c.-6+861_-6+862delinsAT	NP_940839.1:n.-6+861_-6+862delinsAT
XM_017028034.2:c.-486-642_-486-641delinsAT	XP_016883523.1:n.-486-642_-486-641delinsAT
XM_017028035.1:c.-6+484_-6+485delinsAT	XP_016883524.1:n.-6+484_-6+485delinsAT
XM_024451974.1:c.-213-642_-213-641delinsAT	XP_024307742.1:n.-213-642_-213-641delinsAT
NM_001323303.2:c.-116+636_-116+637delinsAT	NP_001310232.1:n.-116+636_-116+637delinsAT
NM_001323304.2:c.-104+861_-104+862delinsAT	NP_001310233.1:n.-104+861_-104+862delinsAT
NM_001323305.2:c.-213-642_-213-641delinsAT	NP_001310234.1:n.-213-642_-213-641delinsAT
NM_003600.4:c.-6+636_-6+637delinsAT	NP_003591.2:n.-6+636_-6+637delinsAT
NM_198433.3:c.-214+636_-214+637delinsAT	NP_940835.1:n.-214+636_-214+637delinsAT
NM_198435.3:c.-6+847_-6+848delinsAT	NP_940837.1:n.-6+847_-6+848delinsAT
NM_198436.3:c.-115-642_-115-641delinsAT	NP_940838.1:n.-115-642_-115-641delinsAT
NM_198437.3:c.-6+861_-6+862delinsAT MANE Select	NP_940839.1:n.-6+861_-6+862delinsAT
NM_198434.3:c.-115-642_-115-641delinsAT	NP_940836.1:n.-115-642_-115-641delinsAT