Canonical Allele Identifier: CA397985228
Gene: AURKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8204927C>A , CM000679.2:g.8204927C>A GRCh38
NC_000017.10:g.8108245C>A , CM000679.1:g.8108245C>A GRCh37
NC_000017.9:g.8048970C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000585124.6:c.979G>T MANE Select ENSP00000463999.1:p.Val327Phe
ENST00000316199.10:c.982G>T ENSP00000313950.6:p.Val328Phe
ENST00000534871.5:c.856G>T ENSP00000443869.1:p.Val286Phe
ENST00000578549.5:c.883G>T ENSP00000462207.1:p.Val295Phe
ENST00000580998.5:c.*326G>T ENSP00000461981.1:n.*326G>T
ENST00000584972.5:c.671G>T
ENST00000585124.5:c.979G>T ENSP00000463999.1:p.Val327Phe
NM_001256834.1:c.856G>T NP_001243763.1:p.Val286Phe
NM_001256834.2:c.856G>T NP_001243763.1:p.Val286Phe
NM_001284526.1:c.982G>T NP_001271455.1:p.Val328Phe
NM_001313950.1:c.979G>T NP_001300879.1:p.Val327Phe
NM_001313951.1:c.856G>T NP_001300880.1:p.Val286Phe
NM_001313952.1:c.859G>T NP_001300881.1:p.Val287Phe
NM_001313953.1:c.883G>T NP_001300882.1:p.Val295Phe
NM_001313954.1:c.523G>T NP_001300883.1:p.Val175Phe
NM_001313955.1:c.475G>T NP_001300884.1:p.Val159Phe
NM_004217.3:c.979G>T NP_004208.2:p.Val327Phe
NR_132730.1:n.959G>T
NR_132731.1:n.844G>T
XM_011524070.1:c.883G>T XP_011522372.1:p.Val295Phe
XM_011524072.1:c.856G>T XP_011522374.1:p.Val286Phe
XR_934118.1:n.1188G>T
NM_001313953.2:c.883G>T NP_001300882.1:p.Val295Phe
XM_011524072.3:c.856G>T XP_011522374.1:p.Val286Phe
XM_017025307.2:c.856G>T XP_016880796.1:p.Val286Phe
XM_017025308.2:c.760G>T XP_016880797.1:p.Val254Phe
XM_017025309.1:c.523G>T XP_016880798.1:p.Val175Phe
XM_017025310.1:c.523G>T XP_016880799.1:p.Val175Phe
XM_017025311.1:c.523G>T XP_016880800.1:p.Val175Phe
NM_004217.4:c.979G>T MANE Select NP_004208.2:p.Val327Phe
NM_001256834.3:c.856G>T NP_001243763.1:p.Val286Phe
NM_001284526.2:c.982G>T NP_001271455.1:p.Val328Phe
NM_001313950.2:c.979G>T NP_001300879.1:p.Val327Phe
NM_001313952.2:c.859G>T NP_001300881.1:p.Val287Phe
NM_001313953.3:c.883G>T NP_001300882.1:p.Val295Phe
NM_001313954.2:c.523G>T NP_001300883.1:p.Val175Phe
NM_001313955.2:c.475G>T NP_001300884.1:p.Val159Phe
NR_132730.2:n.908G>T