Canonical Allele Identifier: CA397985261
Gene: AURKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8204933G>T , CM000679.2:g.8204933G>T GRCh38
NC_000017.10:g.8108251G>T , CM000679.1:g.8108251G>T GRCh37
NC_000017.9:g.8048976G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000585124.6:c.973C>A MANE Select ENSP00000463999.1:p.Pro325Thr
ENST00000316199.10:c.976C>A ENSP00000313950.6:p.Pro326Thr
ENST00000534871.5:c.850C>A ENSP00000443869.1:p.Pro284Thr
ENST00000578549.5:c.877C>A ENSP00000462207.1:p.Pro293Thr
ENST00000580998.5:c.*320C>A ENSP00000461981.1:n.*320C>A
ENST00000584972.5:c.665C>A
ENST00000585124.5:c.973C>A ENSP00000463999.1:p.Pro325Thr
NM_001256834.1:c.850C>A NP_001243763.1:p.Pro284Thr
NM_001256834.2:c.850C>A NP_001243763.1:p.Pro284Thr
NM_001284526.1:c.976C>A NP_001271455.1:p.Pro326Thr
NM_001313950.1:c.973C>A NP_001300879.1:p.Pro325Thr
NM_001313951.1:c.850C>A NP_001300880.1:p.Pro284Thr
NM_001313952.1:c.853C>A NP_001300881.1:p.Pro285Thr
NM_001313953.1:c.877C>A NP_001300882.1:p.Pro293Thr
NM_001313954.1:c.517C>A NP_001300883.1:p.Pro173Thr
NM_001313955.1:c.469C>A NP_001300884.1:p.Pro157Thr
NM_004217.3:c.973C>A NP_004208.2:p.Pro325Thr
NR_132730.1:n.953C>A
NR_132731.1:n.838C>A
XM_011524070.1:c.877C>A XP_011522372.1:p.Pro293Thr
XM_011524072.1:c.850C>A XP_011522374.1:p.Pro284Thr
XR_934118.1:n.1182C>A
NM_001313953.2:c.877C>A NP_001300882.1:p.Pro293Thr
XM_011524072.3:c.850C>A XP_011522374.1:p.Pro284Thr
XM_017025307.2:c.850C>A XP_016880796.1:p.Pro284Thr
XM_017025308.2:c.754C>A XP_016880797.1:p.Pro252Thr
XM_017025309.1:c.517C>A XP_016880798.1:p.Pro173Thr
XM_017025310.1:c.517C>A XP_016880799.1:p.Pro173Thr
XM_017025311.1:c.517C>A XP_016880800.1:p.Pro173Thr
NM_004217.4:c.973C>A MANE Select NP_004208.2:p.Pro325Thr
NM_001256834.3:c.850C>A NP_001243763.1:p.Pro284Thr
NM_001284526.2:c.976C>A NP_001271455.1:p.Pro326Thr
NM_001313950.2:c.973C>A NP_001300879.1:p.Pro325Thr
NM_001313952.2:c.853C>A NP_001300881.1:p.Pro285Thr
NM_001313953.3:c.877C>A NP_001300882.1:p.Pro293Thr
NM_001313954.2:c.517C>A NP_001300883.1:p.Pro173Thr
NM_001313955.2:c.469C>A NP_001300884.1:p.Pro157Thr
NR_132730.2:n.902C>A