Canonical Allele Identifier: CA745785196

Gene: AURKA

Linked Data

• dbSNP Id: rs1453723593
• gnomAD v3: 20-56382598-C-T
• gnomAD v4: 20-56382598-C-T
• MyVariant Identifiers: chr20:g.54957654C>T (hg19) ; chr20:g.56382598C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.56382598C>T , CM000682.2:g.56382598C>T	GRCh38
NC_000020.10:g.54957654C>T , CM000682.1:g.54957654C>T	GRCh37
NC_000020.9:g.54391061C>T	NCBI36
NG_012133.1:g.14698G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395915.8:c.566+387G>A MANE Select	ENSP00000379251.3:n.566+387G>A
ENST00000312783.10:c.566+387G>A	ENSP00000321591.6:n.566+387G>A
ENST00000347343.6:c.566+387G>A	ENSP00000216911.2:n.566+387G>A
ENST00000371356.6:c.566+387G>A	ENSP00000360407.2:n.566+387G>A
ENST00000395907.5:c.566+387G>A	ENSP00000379243.1:n.566+387G>A
ENST00000395911.5:c.566+387G>A	ENSP00000379247.1:n.566+387G>A
ENST00000395913.7:c.566+387G>A	ENSP00000379249.3:n.566+387G>A
ENST00000395914.5:c.566+387G>A	ENSP00000379250.1:n.566+387G>A
ENST00000395915.7:c.566+387G>A	ENSP00000379251.3:n.566+387G>A
ENST00000441357.5:c.566+387G>A	ENSP00000393452.1:n.566+387G>A
NM_003600.2:c.566+387G>A	NP_003591.2:n.566+387G>A
NM_198433.1:c.566+387G>A	NP_940835.1:n.566+387G>A
NM_198434.1:c.566+387G>A	NP_940836.1:n.566+387G>A
NM_198435.1:c.566+387G>A	NP_940837.1:n.566+387G>A
NM_198436.1:c.566+387G>A	NP_940838.1:n.566+387G>A
NM_198437.1:c.566+387G>A	NP_940839.1:n.566+387G>A
XM_005260534.1:c.566+387G>A	XP_005260591.1:n.566+387G>A
XM_006723872.1:c.566+387G>A	XP_006723935.1:n.566+387G>A
XM_011529021.1:c.566+387G>A	XP_011527323.1:n.566+387G>A
NM_001323303.1:c.566+387G>A	NP_001310232.1:n.566+387G>A
NM_001323304.1:c.566+387G>A	NP_001310233.1:n.566+387G>A
NM_001323305.1:c.566+387G>A	NP_001310234.1:n.566+387G>A
NM_003600.3:c.566+387G>A	NP_003591.2:n.566+387G>A
NM_198433.2:c.566+387G>A	NP_940835.1:n.566+387G>A
NM_198434.2:c.566+387G>A	NP_940836.1:n.566+387G>A
NM_198435.2:c.566+387G>A	NP_940837.1:n.566+387G>A
NM_198436.2:c.566+387G>A	NP_940838.1:n.566+387G>A
NM_198437.2:c.566+387G>A	NP_940839.1:n.566+387G>A
XM_017028034.2:c.668+387G>A	XP_016883523.1:n.668+387G>A
XM_017028035.1:c.566+387G>A	XP_016883524.1:n.566+387G>A
XM_024451974.1:c.566+387G>A	XP_024307742.1:n.566+387G>A
NM_001323303.2:c.566+387G>A	NP_001310232.1:n.566+387G>A
NM_001323304.2:c.566+387G>A	NP_001310233.1:n.566+387G>A
NM_001323305.2:c.566+387G>A	NP_001310234.1:n.566+387G>A
NM_003600.4:c.566+387G>A	NP_003591.2:n.566+387G>A
NM_198433.3:c.566+387G>A	NP_940835.1:n.566+387G>A
NM_198435.3:c.566+387G>A	NP_940837.1:n.566+387G>A
NM_198436.3:c.566+387G>A	NP_940838.1:n.566+387G>A
NM_198437.3:c.566+387G>A MANE Select	NP_940839.1:n.566+387G>A
NM_198434.3:c.566+387G>A	NP_940836.1:n.566+387G>A