Canonical Allele Identifier: CA2950981051

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8205000_8205021delinsATCCTGGGCTCCCGTGGGCACA , CM000679.2:g.8205000_8205021delinsATCCTGGGCTCCCGTGGGCACA	GRCh38
NC_000017.10:g.8108318_8108339delinsATCCTGGGCTCCCGTGGGCACA , CM000679.1:g.8108318_8108339delinsATCCTGGGCTCCCGTGGGCACA	GRCh37
NC_000017.9:g.8049043_8049064delinsATCCTGGGCTCCCGTGGGCACA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT MANE Select	ENSP00000463999.1:p.Met298Thr
ENST00000316199.10:c.888_909delinsTGTGCCCACGGGAGCCCAGGAT	ENSP00000313950.6:p.Met299Thr
ENST00000534871.5:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	ENSP00000443869.1:p.Met257Thr
ENST00000578549.5:c.789_810delinsTGTGCCCACGGGAGCCCAGGAT	ENSP00000462207.1:p.Met266Thr
ENST00000578753.1:n.407_428delinsTGTGCCCACGGGAGCCCAGGAT
ENST00000580998.5:c.*232_*253delinsTGTGCCCACGGGAGCCCAGGAT	ENSP00000461981.1:n.*232_*253delinsTGTGCCCACGGGAGCCCAGGAT
ENST00000584972.5:c.577_598delinsTGTGCCCACGGGAGCCCAGGAT
ENST00000585124.5:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT	ENSP00000463999.1:p.Met298Thr
NM_001256834.1:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	NP_001243763.1:p.Met257Thr
NM_001256834.2:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	NP_001243763.1:p.Met257Thr
NM_001284526.1:c.888_909delinsTGTGCCCACGGGAGCCCAGGAT	NP_001271455.1:p.Met299Thr
NM_001313950.1:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300879.1:p.Met298Thr
NM_001313951.1:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300880.1:p.Met257Thr
NM_001313952.1:c.765_786delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300881.1:p.Met258Thr
NM_001313953.1:c.789_810delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300882.1:p.Met266Thr
NM_001313954.1:c.429_450delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300883.1:p.Met146Thr
NM_001313955.1:c.381_402delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300884.1:p.Met130Thr
NM_004217.3:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT	NP_004208.2:p.Met298Thr
NR_132730.1:n.865_886delinsTGTGCCCACGGGAGCCCAGGAT
NR_132731.1:n.750_771delinsTGTGCCCACGGGAGCCCAGGAT
XM_011524070.1:c.789_810delinsTGTGCCCACGGGAGCCCAGGAT	XP_011522372.1:p.Met266Thr
XM_011524072.1:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	XP_011522374.1:p.Met257Thr
XR_934118.1:n.1094_1115delinsTGTGCCCACGGGAGCCCAGGAT
NM_001313953.2:c.789_810delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300882.1:p.Met266Thr
XM_011524072.3:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	XP_011522374.1:p.Met257Thr
XM_017025307.2:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	XP_016880796.1:p.Met257Thr
XM_017025308.2:c.666_687delinsTGTGCCCACGGGAGCCCAGGAT	XP_016880797.1:p.Met225Thr
XM_017025309.1:c.429_450delinsTGTGCCCACGGGAGCCCAGGAT	XP_016880798.1:p.Met146Thr
XM_017025310.1:c.429_450delinsTGTGCCCACGGGAGCCCAGGAT	XP_016880799.1:p.Met146Thr
XM_017025311.1:c.429_450delinsTGTGCCCACGGGAGCCCAGGAT	XP_016880800.1:p.Met146Thr
NM_004217.4:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT MANE Select	NP_004208.2:p.Met298Thr
NM_001256834.3:c.762_783delinsTGTGCCCACGGGAGCCCAGGAT	NP_001243763.1:p.Met257Thr
NM_001284526.2:c.888_909delinsTGTGCCCACGGGAGCCCAGGAT	NP_001271455.1:p.Met299Thr
NM_001313950.2:c.885_906delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300879.1:p.Met298Thr
NM_001313952.2:c.765_786delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300881.1:p.Met258Thr
NM_001313953.3:c.789_810delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300882.1:p.Met266Thr
NM_001313954.2:c.429_450delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300883.1:p.Met146Thr
NM_001313955.2:c.381_402delinsTGTGCCCACGGGAGCCCAGGAT	NP_001300884.1:p.Met130Thr
NR_132730.2:n.814_835delinsTGTGCCCACGGGAGCCCAGGAT