Canonical Allele Identifier: CA397985571
Gene: AURKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8205008C>T , CM000679.2:g.8205008C>T GRCh38
NC_000017.10:g.8108326C>T , CM000679.1:g.8108326C>T GRCh37
NC_000017.9:g.8049051C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000585124.6:c.898G>A MANE Select ENSP00000463999.1:p.Ala300Thr
ENST00000316199.10:c.901G>A ENSP00000313950.6:p.Ala301Thr
ENST00000534871.5:c.775G>A ENSP00000443869.1:p.Ala259Thr
ENST00000578549.5:c.802G>A ENSP00000462207.1:p.Ala268Thr
ENST00000578753.1:n.420G>A
ENST00000580998.5:c.*245G>A ENSP00000461981.1:n.*245G>A
ENST00000584972.5:c.590G>A
ENST00000585124.5:c.898G>A ENSP00000463999.1:p.Ala300Thr
NM_001256834.1:c.775G>A NP_001243763.1:p.Ala259Thr
NM_001256834.2:c.775G>A NP_001243763.1:p.Ala259Thr
NM_001284526.1:c.901G>A NP_001271455.1:p.Ala301Thr
NM_001313950.1:c.898G>A NP_001300879.1:p.Ala300Thr
NM_001313951.1:c.775G>A NP_001300880.1:p.Ala259Thr
NM_001313952.1:c.778G>A NP_001300881.1:p.Ala260Thr
NM_001313953.1:c.802G>A NP_001300882.1:p.Ala268Thr
NM_001313954.1:c.442G>A NP_001300883.1:p.Ala148Thr
NM_001313955.1:c.394G>A NP_001300884.1:p.Ala132Thr
NM_004217.3:c.898G>A NP_004208.2:p.Ala300Thr
NR_132730.1:n.878G>A
NR_132731.1:n.763G>A
XM_011524070.1:c.802G>A XP_011522372.1:p.Ala268Thr
XM_011524072.1:c.775G>A XP_011522374.1:p.Ala259Thr
XR_934118.1:n.1107G>A
NM_001313953.2:c.802G>A NP_001300882.1:p.Ala268Thr
XM_011524072.3:c.775G>A XP_011522374.1:p.Ala259Thr
XM_017025307.2:c.775G>A XP_016880796.1:p.Ala259Thr
XM_017025308.2:c.679G>A XP_016880797.1:p.Ala227Thr
XM_017025309.1:c.442G>A XP_016880798.1:p.Ala148Thr
XM_017025310.1:c.442G>A XP_016880799.1:p.Ala148Thr
XM_017025311.1:c.442G>A XP_016880800.1:p.Ala148Thr
NM_004217.4:c.898G>A MANE Select NP_004208.2:p.Ala300Thr
NM_001256834.3:c.775G>A NP_001243763.1:p.Ala259Thr
NM_001284526.2:c.901G>A NP_001271455.1:p.Ala301Thr
NM_001313950.2:c.898G>A NP_001300879.1:p.Ala300Thr
NM_001313952.2:c.778G>A NP_001300881.1:p.Ala260Thr
NM_001313953.3:c.802G>A NP_001300882.1:p.Ala268Thr
NM_001313954.2:c.442G>A NP_001300883.1:p.Ala148Thr
NM_001313955.2:c.394G>A NP_001300884.1:p.Ala132Thr
NR_132730.2:n.827G>A