Canonical Allele Identifier: CA397985248
Gene: AURKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8204930A>G , CM000679.2:g.8204930A>G GRCh38
NC_000017.10:g.8108248A>G , CM000679.1:g.8108248A>G GRCh37
NC_000017.9:g.8048973A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000585124.6:c.976T>C MANE Select ENSP00000463999.1:p.Trp326Arg
ENST00000316199.10:c.979T>C ENSP00000313950.6:p.Trp327Arg
ENST00000534871.5:c.853T>C ENSP00000443869.1:p.Trp285Arg
ENST00000578549.5:c.880T>C ENSP00000462207.1:p.Trp294Arg
ENST00000580998.5:c.*323T>C ENSP00000461981.1:n.*323T>C
ENST00000584972.5:c.668T>C
ENST00000585124.5:c.976T>C ENSP00000463999.1:p.Trp326Arg
NM_001256834.1:c.853T>C NP_001243763.1:p.Trp285Arg
NM_001256834.2:c.853T>C NP_001243763.1:p.Trp285Arg
NM_001284526.1:c.979T>C NP_001271455.1:p.Trp327Arg
NM_001313950.1:c.976T>C NP_001300879.1:p.Trp326Arg
NM_001313951.1:c.853T>C NP_001300880.1:p.Trp285Arg
NM_001313952.1:c.856T>C NP_001300881.1:p.Trp286Arg
NM_001313953.1:c.880T>C NP_001300882.1:p.Trp294Arg
NM_001313954.1:c.520T>C NP_001300883.1:p.Trp174Arg
NM_001313955.1:c.472T>C NP_001300884.1:p.Trp158Arg
NM_004217.3:c.976T>C NP_004208.2:p.Trp326Arg
NR_132730.1:n.956T>C
NR_132731.1:n.841T>C
XM_011524070.1:c.880T>C XP_011522372.1:p.Trp294Arg
XM_011524072.1:c.853T>C XP_011522374.1:p.Trp285Arg
XR_934118.1:n.1185T>C
NM_001313953.2:c.880T>C NP_001300882.1:p.Trp294Arg
XM_011524072.3:c.853T>C XP_011522374.1:p.Trp285Arg
XM_017025307.2:c.853T>C XP_016880796.1:p.Trp285Arg
XM_017025308.2:c.757T>C XP_016880797.1:p.Trp253Arg
XM_017025309.1:c.520T>C XP_016880798.1:p.Trp174Arg
XM_017025310.1:c.520T>C XP_016880799.1:p.Trp174Arg
XM_017025311.1:c.520T>C XP_016880800.1:p.Trp174Arg
NM_004217.4:c.976T>C MANE Select NP_004208.2:p.Trp326Arg
NM_001256834.3:c.853T>C NP_001243763.1:p.Trp285Arg
NM_001284526.2:c.979T>C NP_001271455.1:p.Trp327Arg
NM_001313950.2:c.976T>C NP_001300879.1:p.Trp326Arg
NM_001313952.2:c.856T>C NP_001300881.1:p.Trp286Arg
NM_001313953.3:c.880T>C NP_001300882.1:p.Trp294Arg
NM_001313954.2:c.520T>C NP_001300883.1:p.Trp174Arg
NM_001313955.2:c.472T>C NP_001300884.1:p.Trp158Arg
NR_132730.2:n.905T>C