Canonical Allele Identifier: CA2816785131
Gene: AURKA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.56391325G>A , CM000682.2:g.56391325G>A GRCh38
NC_000020.10:g.54966381G>A , CM000682.1:g.54966381G>A GRCh37
NC_000020.9:g.54399788G>A NCBI36
NG_012133.1:g.5971C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395915.8:c.-6+843C>T MANE Select ENSP00000379251.3:n.-6+843C>T
ENST00000312783.10:c.-115-660C>T ENSP00000321591.6:n.-115-660C>T
ENST00000347343.6:c.-6+618C>T ENSP00000216911.2:n.-6+618C>T
ENST00000371356.6:c.-104+843C>T ENSP00000360407.2:n.-104+843C>T
ENST00000395907.5:c.-6+843C>T ENSP00000379243.1:n.-6+843C>T
ENST00000395911.5:c.-104+829C>T ENSP00000379247.1:n.-104+829C>T
ENST00000395913.7:c.-6+829C>T ENSP00000379249.3:n.-6+829C>T
ENST00000395914.5:c.-115-660C>T ENSP00000379250.1:n.-115-660C>T
ENST00000395915.7:c.-6+843C>T ENSP00000379251.3:n.-6+843C>T
ENST00000420474.5:c.-213-660C>T ENSP00000388073.1:n.-213-660C>T
ENST00000422322.5:c.-116+618C>T ENSP00000405042.1:n.-116+618C>T
ENST00000441357.5:c.-115-660C>T ENSP00000393452.1:n.-115-660C>T
ENST00000451915.1:c.-310-660C>T ENSP00000401358.1:n.-310-660C>T
ENST00000456249.5:c.-214+618C>T ENSP00000405170.1:n.-214+618C>T
NM_003600.2:c.-6+618C>T NP_003591.2:n.-6+618C>T
NM_198433.1:c.-214+618C>T NP_940835.1:n.-214+618C>T
NM_198434.1:c.-115-660C>T NP_940836.1:n.-115-660C>T
NM_198435.1:c.-6+829C>T NP_940837.1:n.-6+829C>T
NM_198436.1:c.-115-660C>T NP_940838.1:n.-115-660C>T
NM_198437.1:c.-6+843C>T NP_940839.1:n.-6+843C>T
XM_005260534.1:c.-116+618C>T XP_005260591.1:n.-116+618C>T
XM_006723872.1:c.-104+618C>T XP_006723935.1:n.-104+618C>T
NM_001323303.1:c.-116+618C>T NP_001310232.1:n.-116+618C>T
NM_001323304.1:c.-104+843C>T NP_001310233.1:n.-104+843C>T
NM_001323305.1:c.-213-660C>T NP_001310234.1:n.-213-660C>T
NM_003600.3:c.-6+618C>T NP_003591.2:n.-6+618C>T
NM_198433.2:c.-214+618C>T NP_940835.1:n.-214+618C>T
NM_198434.2:c.-115-660C>T NP_940836.1:n.-115-660C>T
NM_198435.2:c.-6+829C>T NP_940837.1:n.-6+829C>T
NM_198436.2:c.-115-660C>T NP_940838.1:n.-115-660C>T
NM_198437.2:c.-6+843C>T NP_940839.1:n.-6+843C>T
XM_017028034.2:c.-486-660C>T XP_016883523.1:n.-486-660C>T
XM_017028035.1:c.-6+466C>T XP_016883524.1:n.-6+466C>T
XM_024451974.1:c.-213-660C>T XP_024307742.1:n.-213-660C>T
NM_001323303.2:c.-116+618C>T NP_001310232.1:n.-116+618C>T
NM_001323304.2:c.-104+843C>T NP_001310233.1:n.-104+843C>T
NM_001323305.2:c.-213-660C>T NP_001310234.1:n.-213-660C>T
NM_003600.4:c.-6+618C>T NP_003591.2:n.-6+618C>T
NM_198433.3:c.-214+618C>T NP_940835.1:n.-214+618C>T
NM_198435.3:c.-6+829C>T NP_940837.1:n.-6+829C>T
NM_198436.3:c.-115-660C>T NP_940838.1:n.-115-660C>T
NM_198437.3:c.-6+843C>T MANE Select NP_940839.1:n.-6+843C>T
NM_198434.3:c.-115-660C>T NP_940836.1:n.-115-660C>T