Canonical Allele Identifier: CA2246210478

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204910C= , CM000679.2:g.8204910C=	GRCh38
NC_000017.10:g.8108228C= , CM000679.1:g.8108228C=	GRCh37
NC_000017.9:g.8048953C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.996G= MANE Select	ENSP00000463999.1:p.Arg332=
ENST00000316199.10:c.999G=	ENSP00000313950.6:p.Arg333=
ENST00000534871.5:c.873G=	ENSP00000443869.1:p.Arg291=
ENST00000578549.5:c.900G=	ENSP00000462207.1:p.Arg300=
ENST00000580998.5:c.*343G=	ENSP00000461981.1:n.*343G=
ENST00000584972.5:c.688G=
ENST00000585124.5:c.996G=	ENSP00000463999.1:p.Arg332=
NM_001256834.1:c.873G=	NP_001243763.1:p.Arg291=
NM_001256834.2:c.873G=	NP_001243763.1:p.Arg291=
NM_001284526.1:c.999G=	NP_001271455.1:p.Arg333=
NM_001313950.1:c.996G=	NP_001300879.1:p.Arg332=
NM_001313951.1:c.873G=	NP_001300880.1:p.Arg291=
NM_001313952.1:c.876G=	NP_001300881.1:p.Arg292=
NM_001313953.1:c.900G=	NP_001300882.1:p.Arg300=
NM_001313954.1:c.540G=	NP_001300883.1:p.Arg180=
NM_001313955.1:c.492G=	NP_001300884.1:p.Arg164=
NM_004217.3:c.996G=	NP_004208.2:p.Arg332=
NR_132730.1:n.976G=
NR_132731.1:n.861G=
XM_011524070.1:c.900G=	XP_011522372.1:p.Arg300=
XM_011524072.1:c.873G=	XP_011522374.1:p.Arg291=
XR_934118.1:n.1205G=
NM_001313953.2:c.900G=	NP_001300882.1:p.Arg300=
XM_011524072.3:c.873G=	XP_011522374.1:p.Arg291=
XM_017025307.2:c.873G=	XP_016880796.1:p.Arg291=
XM_017025308.2:c.777G=	XP_016880797.1:p.Arg259=
XM_017025309.1:c.540G=	XP_016880798.1:p.Arg180=
XM_017025310.1:c.540G=	XP_016880799.1:p.Arg180=
XM_017025311.1:c.540G=	XP_016880800.1:p.Arg180=
NM_004217.4:c.996G= MANE Select	NP_004208.2:p.Arg332=
NM_001256834.3:c.873G=	NP_001243763.1:p.Arg291=
NM_001284526.2:c.999G=	NP_001271455.1:p.Arg333=
NM_001313950.2:c.996G=	NP_001300879.1:p.Arg332=
NM_001313952.2:c.876G=	NP_001300881.1:p.Arg292=
NM_001313953.3:c.900G=	NP_001300882.1:p.Arg300=
NM_001313954.2:c.540G=	NP_001300883.1:p.Arg180=
NM_001313955.2:c.492G=	NP_001300884.1:p.Arg164=
NR_132730.2:n.925G=