Canonical Allele Identifier: CA2246210479

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204911C= , CM000679.2:g.8204911C=	GRCh38
NC_000017.10:g.8108229C= , CM000679.1:g.8108229C=	GRCh37
NC_000017.9:g.8048954C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.995G= MANE Select	ENSP00000463999.1:p.Arg332=
ENST00000316199.10:c.998G=	ENSP00000313950.6:p.Arg333=
ENST00000534871.5:c.872G=	ENSP00000443869.1:p.Arg291=
ENST00000578549.5:c.899G=	ENSP00000462207.1:p.Arg300=
ENST00000580998.5:c.*342G=	ENSP00000461981.1:n.*342G=
ENST00000584972.5:c.687G=
ENST00000585124.5:c.995G=	ENSP00000463999.1:p.Arg332=
NM_001256834.1:c.872G=	NP_001243763.1:p.Arg291=
NM_001256834.2:c.872G=	NP_001243763.1:p.Arg291=
NM_001284526.1:c.998G=	NP_001271455.1:p.Arg333=
NM_001313950.1:c.995G=	NP_001300879.1:p.Arg332=
NM_001313951.1:c.872G=	NP_001300880.1:p.Arg291=
NM_001313952.1:c.875G=	NP_001300881.1:p.Arg292=
NM_001313953.1:c.899G=	NP_001300882.1:p.Arg300=
NM_001313954.1:c.539G=	NP_001300883.1:p.Arg180=
NM_001313955.1:c.491G=	NP_001300884.1:p.Arg164=
NM_004217.3:c.995G=	NP_004208.2:p.Arg332=
NR_132730.1:n.975G=
NR_132731.1:n.860G=
XM_011524070.1:c.899G=	XP_011522372.1:p.Arg300=
XM_011524072.1:c.872G=	XP_011522374.1:p.Arg291=
XR_934118.1:n.1204G=
NM_001313953.2:c.899G=	NP_001300882.1:p.Arg300=
XM_011524072.3:c.872G=	XP_011522374.1:p.Arg291=
XM_017025307.2:c.872G=	XP_016880796.1:p.Arg291=
XM_017025308.2:c.776G=	XP_016880797.1:p.Arg259=
XM_017025309.1:c.539G=	XP_016880798.1:p.Arg180=
XM_017025310.1:c.539G=	XP_016880799.1:p.Arg180=
XM_017025311.1:c.539G=	XP_016880800.1:p.Arg180=
NM_004217.4:c.995G= MANE Select	NP_004208.2:p.Arg332=
NM_001256834.3:c.872G=	NP_001243763.1:p.Arg291=
NM_001284526.2:c.998G=	NP_001271455.1:p.Arg333=
NM_001313950.2:c.995G=	NP_001300879.1:p.Arg332=
NM_001313952.2:c.875G=	NP_001300881.1:p.Arg292=
NM_001313953.3:c.899G=	NP_001300882.1:p.Arg300=
NM_001313954.2:c.539G=	NP_001300883.1:p.Arg180=
NM_001313955.2:c.491G=	NP_001300884.1:p.Arg164=
NR_132730.2:n.924G=