Canonical Allele Identifier: CA2576162508

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204782A>T , CM000679.2:g.8204782A>T	GRCh38
NC_000017.10:g.8108100A>T , CM000679.1:g.8108100A>T	GRCh37
NC_000017.9:g.8048825A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.*89T>A MANE Select	ENSP00000463999.1:n.*89T>A
ENST00000316199.10:c.*89T>A	ENSP00000313950.6:n.*89T>A
ENST00000534871.5:c.*89T>A	ENSP00000443869.1:n.*89T>A
ENST00000585124.5:c.*89T>A	ENSP00000463999.1:n.*89T>A
NM_001256834.1:c.*89T>A	NP_001243763.1:n.*89T>A
NM_001256834.2:c.*89T>A	NP_001243763.1:n.*89T>A
NM_001284526.1:c.*89T>A	NP_001271455.1:n.*89T>A
NM_001313950.1:c.*89T>A	NP_001300879.1:n.*89T>A
NM_001313951.1:c.*89T>A	NP_001300880.1:n.*89T>A
NM_001313952.1:c.*89T>A	NP_001300881.1:n.*89T>A
NM_001313953.1:c.*89T>A	NP_001300882.1:n.*89T>A
NM_001313954.1:c.*89T>A	NP_001300883.1:n.*89T>A
NM_001313955.1:c.*89T>A	NP_001300884.1:n.*89T>A
NM_004217.3:c.*89T>A	NP_004208.2:n.*89T>A
NR_132730.1:n.1104T>A
NR_132731.1:n.989T>A
XM_011524070.1:c.*89T>A	XP_011522372.1:n.*89T>A
XM_011524072.1:c.*89T>A	XP_011522374.1:n.*89T>A
XR_934118.1:n.1333T>A
NM_001313953.2:c.*89T>A	NP_001300882.1:n.*89T>A
XM_011524072.3:c.*89T>A	XP_011522374.1:n.*89T>A
XM_017025307.2:c.*89T>A	XP_016880796.1:n.*89T>A
XM_017025308.2:c.*89T>A	XP_016880797.1:n.*89T>A
XM_017025309.1:c.*89T>A	XP_016880798.1:n.*89T>A
XM_017025310.1:c.*89T>A	XP_016880799.1:n.*89T>A
XM_017025311.1:c.*89T>A	XP_016880800.1:n.*89T>A
NM_004217.4:c.*89T>A MANE Select	NP_004208.2:n.*89T>A
NM_001256834.3:c.*89T>A	NP_001243763.1:n.*89T>A
NM_001284526.2:c.*89T>A	NP_001271455.1:n.*89T>A
NM_001313950.2:c.*89T>A	NP_001300879.1:n.*89T>A
NM_001313952.2:c.*89T>A	NP_001300881.1:n.*89T>A
NM_001313953.3:c.*89T>A	NP_001300882.1:n.*89T>A
NM_001313954.2:c.*89T>A	NP_001300883.1:n.*89T>A
NM_001313955.2:c.*89T>A	NP_001300884.1:n.*89T>A
NR_132730.2:n.1053T>A