Canonical Allele Identifier: CA409699404

Gene: AURKA

Linked Data

• dbSNP Id: rs2146204816
• MyVariant Identifiers: chr20:g.54961451C>T (hg19) ; chr20:g.56386395C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56386395C>T , CM000682.2:g.56386395C>T	GRCh38
NC_000020.10:g.54961451C>T , CM000682.1:g.54961451C>T	GRCh37
NC_000020.9:g.54394858C>T	NCBI36
NG_012133.1:g.10901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395915.8:c.181G>A MANE Select	ENSP00000379251.3:p.Ala61Thr
ENST00000312783.10:c.181G>A	ENSP00000321591.6:p.Ala61Thr
ENST00000347343.6:c.181G>A	ENSP00000216911.2:p.Ala61Thr
ENST00000371356.6:c.181G>A	ENSP00000360407.2:p.Ala61Thr
ENST00000395907.5:c.181G>A	ENSP00000379243.1:p.Ala61Thr
ENST00000395911.5:c.181G>A	ENSP00000379247.1:p.Ala61Thr
ENST00000395913.7:c.181G>A	ENSP00000379249.3:p.Ala61Thr
ENST00000395914.5:c.181G>A	ENSP00000379250.1:p.Ala61Thr
ENST00000395915.7:c.181G>A	ENSP00000379251.3:p.Ala61Thr
ENST00000420474.5:c.181G>A	ENSP00000388073.1:p.Ala61Thr
ENST00000422322.5:c.181G>A	ENSP00000405042.1:p.Ala61Thr
ENST00000441357.5:c.181G>A	ENSP00000393452.1:p.Ala61Thr
ENST00000451915.1:c.181G>A	ENSP00000401358.1:p.Ala61Thr
ENST00000456249.5:c.181G>A	ENSP00000405170.1:p.Ala61Thr
NM_003600.2:c.181G>A	NP_003591.2:p.Ala61Thr
NM_198433.1:c.181G>A	NP_940835.1:p.Ala61Thr
NM_198434.1:c.181G>A	NP_940836.1:p.Ala61Thr
NM_198435.1:c.181G>A	NP_940837.1:p.Ala61Thr
NM_198436.1:c.181G>A	NP_940838.1:p.Ala61Thr
NM_198437.1:c.181G>A	NP_940839.1:p.Ala61Thr
XM_005260534.1:c.181G>A	XP_005260591.1:p.Ala61Thr
XM_006723872.1:c.181G>A	XP_006723935.1:p.Ala61Thr
XM_011529021.1:c.181G>A	XP_011527323.1:p.Ala61Thr
NM_001323303.1:c.181G>A	NP_001310232.1:p.Ala61Thr
NM_001323304.1:c.181G>A	NP_001310233.1:p.Ala61Thr
NM_001323305.1:c.181G>A	NP_001310234.1:p.Ala61Thr
NM_003600.3:c.181G>A	NP_003591.2:p.Ala61Thr
NM_198433.2:c.181G>A	NP_940835.1:p.Ala61Thr
NM_198434.2:c.181G>A	NP_940836.1:p.Ala61Thr
NM_198435.2:c.181G>A	NP_940837.1:p.Ala61Thr
NM_198436.2:c.181G>A	NP_940838.1:p.Ala61Thr
NM_198437.2:c.181G>A	NP_940839.1:p.Ala61Thr
XM_017028034.2:c.283G>A	XP_016883523.1:p.Ala95Thr
XM_017028035.1:c.181G>A	XP_016883524.1:p.Ala61Thr
XM_024451974.1:c.181G>A	XP_024307742.1:p.Ala61Thr
NM_001323303.2:c.181G>A	NP_001310232.1:p.Ala61Thr
NM_001323304.2:c.181G>A	NP_001310233.1:p.Ala61Thr
NM_001323305.2:c.181G>A	NP_001310234.1:p.Ala61Thr
NM_003600.4:c.181G>A	NP_003591.2:p.Ala61Thr
NM_198433.3:c.181G>A	NP_940835.1:p.Ala61Thr
NM_198435.3:c.181G>A	NP_940837.1:p.Ala61Thr
NM_198436.3:c.181G>A	NP_940838.1:p.Ala61Thr
NM_198437.3:c.181G>A MANE Select	NP_940839.1:p.Ala61Thr
NM_198434.3:c.181G>A	NP_940836.1:p.Ala61Thr