Canonical Allele Identifier: CA397985140
Gene: AURKB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8204896G>C , CM000679.2:g.8204896G>C GRCh38
NC_000017.10:g.8108214G>C , CM000679.1:g.8108214G>C GRCh37
NC_000017.9:g.8048939G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000585124.6:c.1010C>G MANE Select ENSP00000463999.1:p.Pro337Arg
ENST00000316199.10:c.1013C>G ENSP00000313950.6:p.Pro338Arg
ENST00000534871.5:c.887C>G ENSP00000443869.1:p.Pro296Arg
ENST00000578549.5:c.914C>G ENSP00000462207.1:p.Pro305Arg
ENST00000584972.5:c.702C>G
ENST00000585124.5:c.1010C>G ENSP00000463999.1:p.Pro337Arg
NM_001256834.1:c.887C>G NP_001243763.1:p.Pro296Arg
NM_001256834.2:c.887C>G NP_001243763.1:p.Pro296Arg
NM_001284526.1:c.1013C>G NP_001271455.1:p.Pro338Arg
NM_001313950.1:c.1010C>G NP_001300879.1:p.Pro337Arg
NM_001313951.1:c.887C>G NP_001300880.1:p.Pro296Arg
NM_001313952.1:c.890C>G NP_001300881.1:p.Pro297Arg
NM_001313953.1:c.914C>G NP_001300882.1:p.Pro305Arg
NM_001313954.1:c.554C>G NP_001300883.1:p.Pro185Arg
NM_001313955.1:c.506C>G NP_001300884.1:p.Pro169Arg
NM_004217.3:c.1010C>G NP_004208.2:p.Pro337Arg
NR_132730.1:n.990C>G
NR_132731.1:n.875C>G
XM_011524070.1:c.914C>G XP_011522372.1:p.Pro305Arg
XM_011524072.1:c.887C>G XP_011522374.1:p.Pro296Arg
XR_934118.1:n.1219C>G
NM_001313953.2:c.914C>G NP_001300882.1:p.Pro305Arg
XM_011524072.3:c.887C>G XP_011522374.1:p.Pro296Arg
XM_017025307.2:c.887C>G XP_016880796.1:p.Pro296Arg
XM_017025308.2:c.791C>G XP_016880797.1:p.Pro264Arg
XM_017025309.1:c.554C>G XP_016880798.1:p.Pro185Arg
XM_017025310.1:c.554C>G XP_016880799.1:p.Pro185Arg
XM_017025311.1:c.554C>G XP_016880800.1:p.Pro185Arg
NM_004217.4:c.1010C>G MANE Select NP_004208.2:p.Pro337Arg
NM_001256834.3:c.887C>G NP_001243763.1:p.Pro296Arg
NM_001284526.2:c.1013C>G NP_001271455.1:p.Pro338Arg
NM_001313950.2:c.1010C>G NP_001300879.1:p.Pro337Arg
NM_001313952.2:c.890C>G NP_001300881.1:p.Pro297Arg
NM_001313953.3:c.914C>G NP_001300882.1:p.Pro305Arg
NM_001313954.2:c.554C>G NP_001300883.1:p.Pro185Arg
NM_001313955.2:c.506C>G NP_001300884.1:p.Pro169Arg
NR_132730.2:n.939C>G