Canonical Allele Identifier: CA497768557

Gene: AURKB

Linked Data

• MyVariant Identifiers: chr17:g.8108237G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204919G>C , CM000679.2:g.8204919G>C	GRCh38
NC_000017.10:g.8108237G>C , CM000679.1:g.8108237G>C	GRCh37
NC_000017.9:g.8048962G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.987C>G MANE Select	ENSP00000463999.1:p.Ala329=
ENST00000316199.10:c.990C>G	ENSP00000313950.6:p.Ala330=
ENST00000534871.5:c.864C>G	ENSP00000443869.1:p.Ala288=
ENST00000578549.5:c.891C>G	ENSP00000462207.1:p.Ala297=
ENST00000580998.5:c.*334C>G	ENSP00000461981.1:n.*334C>G
ENST00000584972.5:c.679C>G
ENST00000585124.5:c.987C>G	ENSP00000463999.1:p.Ala329=
NM_001256834.1:c.864C>G	NP_001243763.1:p.Ala288=
NM_001256834.2:c.864C>G	NP_001243763.1:p.Ala288=
NM_001284526.1:c.990C>G	NP_001271455.1:p.Ala330=
NM_001313950.1:c.987C>G	NP_001300879.1:p.Ala329=
NM_001313951.1:c.864C>G	NP_001300880.1:p.Ala288=
NM_001313952.1:c.867C>G	NP_001300881.1:p.Ala289=
NM_001313953.1:c.891C>G	NP_001300882.1:p.Ala297=
NM_001313954.1:c.531C>G	NP_001300883.1:p.Ala177=
NM_001313955.1:c.483C>G	NP_001300884.1:p.Ala161=
NM_004217.3:c.987C>G	NP_004208.2:p.Ala329=
NR_132730.1:n.967C>G
NR_132731.1:n.852C>G
XM_011524070.1:c.891C>G	XP_011522372.1:p.Ala297=
XM_011524072.1:c.864C>G	XP_011522374.1:p.Ala288=
XR_934118.1:n.1196C>G
NM_001313953.2:c.891C>G	NP_001300882.1:p.Ala297=
XM_011524072.3:c.864C>G	XP_011522374.1:p.Ala288=
XM_017025307.2:c.864C>G	XP_016880796.1:p.Ala288=
XM_017025308.2:c.768C>G	XP_016880797.1:p.Ala256=
XM_017025309.1:c.531C>G	XP_016880798.1:p.Ala177=
XM_017025310.1:c.531C>G	XP_016880799.1:p.Ala177=
XM_017025311.1:c.531C>G	XP_016880800.1:p.Ala177=
NM_004217.4:c.987C>G MANE Select	NP_004208.2:p.Ala329=
NM_001256834.3:c.864C>G	NP_001243763.1:p.Ala288=
NM_001284526.2:c.990C>G	NP_001271455.1:p.Ala330=
NM_001313950.2:c.987C>G	NP_001300879.1:p.Ala329=
NM_001313952.2:c.867C>G	NP_001300881.1:p.Ala289=
NM_001313953.3:c.891C>G	NP_001300882.1:p.Ala297=
NM_001313954.2:c.531C>G	NP_001300883.1:p.Ala177=
NM_001313955.2:c.483C>G	NP_001300884.1:p.Ala161=
NR_132730.2:n.916C>G