Canonical Allele Identifier: CA2371346834
Gene: AURKA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.56391320G= , CM000682.2:g.56391320G= GRCh38
NC_000020.10:g.54966376G= , CM000682.1:g.54966376G= GRCh37
NC_000020.9:g.54399783G= NCBI36
NG_012133.1:g.5976C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395915.8:c.-6+848C= MANE Select ENSP00000379251.3:n.-6+848C=
ENST00000312783.10:c.-115-655C= ENSP00000321591.6:n.-115-655C=
ENST00000347343.6:c.-6+623C= ENSP00000216911.2:n.-6+623C=
ENST00000371356.6:c.-104+848C= ENSP00000360407.2:n.-104+848C=
ENST00000395907.5:c.-6+848C= ENSP00000379243.1:n.-6+848C=
ENST00000395911.5:c.-104+834C= ENSP00000379247.1:n.-104+834C=
ENST00000395913.7:c.-6+834C= ENSP00000379249.3:n.-6+834C=
ENST00000395914.5:c.-115-655C= ENSP00000379250.1:n.-115-655C=
ENST00000395915.7:c.-6+848C= ENSP00000379251.3:n.-6+848C=
ENST00000420474.5:c.-213-655C= ENSP00000388073.1:n.-213-655C=
ENST00000422322.5:c.-116+623C= ENSP00000405042.1:n.-116+623C=
ENST00000441357.5:c.-115-655C= ENSP00000393452.1:n.-115-655C=
ENST00000451915.1:c.-310-655C= ENSP00000401358.1:n.-310-655C=
ENST00000456249.5:c.-214+623C= ENSP00000405170.1:n.-214+623C=
NM_003600.2:c.-6+623C= NP_003591.2:n.-6+623C=
NM_198433.1:c.-214+623C= NP_940835.1:n.-214+623C=
NM_198434.1:c.-115-655C= NP_940836.1:n.-115-655C=
NM_198435.1:c.-6+834C= NP_940837.1:n.-6+834C=
NM_198436.1:c.-115-655C= NP_940838.1:n.-115-655C=
NM_198437.1:c.-6+848C= NP_940839.1:n.-6+848C=
XM_005260534.1:c.-116+623C= XP_005260591.1:n.-116+623C=
XM_006723872.1:c.-104+623C= XP_006723935.1:n.-104+623C=
NM_001323303.1:c.-116+623C= NP_001310232.1:n.-116+623C=
NM_001323304.1:c.-104+848C= NP_001310233.1:n.-104+848C=
NM_001323305.1:c.-213-655C= NP_001310234.1:n.-213-655C=
NM_003600.3:c.-6+623C= NP_003591.2:n.-6+623C=
NM_198433.2:c.-214+623C= NP_940835.1:n.-214+623C=
NM_198434.2:c.-115-655C= NP_940836.1:n.-115-655C=
NM_198435.2:c.-6+834C= NP_940837.1:n.-6+834C=
NM_198436.2:c.-115-655C= NP_940838.1:n.-115-655C=
NM_198437.2:c.-6+848C= NP_940839.1:n.-6+848C=
XM_017028034.2:c.-486-655C= XP_016883523.1:n.-486-655C=
XM_017028035.1:c.-6+471C= XP_016883524.1:n.-6+471C=
XM_024451974.1:c.-213-655C= XP_024307742.1:n.-213-655C=
NM_001323303.2:c.-116+623C= NP_001310232.1:n.-116+623C=
NM_001323304.2:c.-104+848C= NP_001310233.1:n.-104+848C=
NM_001323305.2:c.-213-655C= NP_001310234.1:n.-213-655C=
NM_003600.4:c.-6+623C= NP_003591.2:n.-6+623C=
NM_198433.3:c.-214+623C= NP_940835.1:n.-214+623C=
NM_198435.3:c.-6+834C= NP_940837.1:n.-6+834C=
NM_198436.3:c.-115-655C= NP_940838.1:n.-115-655C=
NM_198437.3:c.-6+848C= MANE Select NP_940839.1:n.-6+848C=
NM_198434.3:c.-115-655C= NP_940836.1:n.-115-655C=