Canonical Allele Identifier: CA2246210486

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204921C= , CM000679.2:g.8204921C=	GRCh38
NC_000017.10:g.8108239C= , CM000679.1:g.8108239C=	GRCh37
NC_000017.9:g.8048964C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.985G= MANE Select	ENSP00000463999.1:p.Ala329=
ENST00000316199.10:c.988G=	ENSP00000313950.6:p.Ala330=
ENST00000534871.5:c.862G=	ENSP00000443869.1:p.Ala288=
ENST00000578549.5:c.889G=	ENSP00000462207.1:p.Ala297=
ENST00000580998.5:c.*332G=	ENSP00000461981.1:n.*332G=
ENST00000584972.5:c.677G=
ENST00000585124.5:c.985G=	ENSP00000463999.1:p.Ala329=
NM_001256834.1:c.862G=	NP_001243763.1:p.Ala288=
NM_001256834.2:c.862G=	NP_001243763.1:p.Ala288=
NM_001284526.1:c.988G=	NP_001271455.1:p.Ala330=
NM_001313950.1:c.985G=	NP_001300879.1:p.Ala329=
NM_001313951.1:c.862G=	NP_001300880.1:p.Ala288=
NM_001313952.1:c.865G=	NP_001300881.1:p.Ala289=
NM_001313953.1:c.889G=	NP_001300882.1:p.Ala297=
NM_001313954.1:c.529G=	NP_001300883.1:p.Ala177=
NM_001313955.1:c.481G=	NP_001300884.1:p.Ala161=
NM_004217.3:c.985G=	NP_004208.2:p.Ala329=
NR_132730.1:n.965G=
NR_132731.1:n.850G=
XM_011524070.1:c.889G=	XP_011522372.1:p.Ala297=
XM_011524072.1:c.862G=	XP_011522374.1:p.Ala288=
XR_934118.1:n.1194G=
NM_001313953.2:c.889G=	NP_001300882.1:p.Ala297=
XM_011524072.3:c.862G=	XP_011522374.1:p.Ala288=
XM_017025307.2:c.862G=	XP_016880796.1:p.Ala288=
XM_017025308.2:c.766G=	XP_016880797.1:p.Ala256=
XM_017025309.1:c.529G=	XP_016880798.1:p.Ala177=
XM_017025310.1:c.529G=	XP_016880799.1:p.Ala177=
XM_017025311.1:c.529G=	XP_016880800.1:p.Ala177=
NM_004217.4:c.985G= MANE Select	NP_004208.2:p.Ala329=
NM_001256834.3:c.862G=	NP_001243763.1:p.Ala288=
NM_001284526.2:c.988G=	NP_001271455.1:p.Ala330=
NM_001313950.2:c.985G=	NP_001300879.1:p.Ala329=
NM_001313952.2:c.865G=	NP_001300881.1:p.Ala289=
NM_001313953.3:c.889G=	NP_001300882.1:p.Ala297=
NM_001313954.2:c.529G=	NP_001300883.1:p.Ala177=
NM_001313955.2:c.481G=	NP_001300884.1:p.Ala161=
NR_132730.2:n.914G=