Canonical Allele Identifier: CA2246210488

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204924G= , CM000679.2:g.8204924G=	GRCh38
NC_000017.10:g.8108242G= , CM000679.1:g.8108242G=	GRCh37
NC_000017.9:g.8048967G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.982C= MANE Select	ENSP00000463999.1:p.Arg328=
ENST00000316199.10:c.985C=	ENSP00000313950.6:p.Arg329=
ENST00000534871.5:c.859C=	ENSP00000443869.1:p.Arg287=
ENST00000578549.5:c.886C=	ENSP00000462207.1:p.Arg296=
ENST00000580998.5:c.*329C=	ENSP00000461981.1:n.*329C=
ENST00000584972.5:c.674C=
ENST00000585124.5:c.982C=	ENSP00000463999.1:p.Arg328=
NM_001256834.1:c.859C=	NP_001243763.1:p.Arg287=
NM_001256834.2:c.859C=	NP_001243763.1:p.Arg287=
NM_001284526.1:c.985C=	NP_001271455.1:p.Arg329=
NM_001313950.1:c.982C=	NP_001300879.1:p.Arg328=
NM_001313951.1:c.859C=	NP_001300880.1:p.Arg287=
NM_001313952.1:c.862C=	NP_001300881.1:p.Arg288=
NM_001313953.1:c.886C=	NP_001300882.1:p.Arg296=
NM_001313954.1:c.526C=	NP_001300883.1:p.Arg176=
NM_001313955.1:c.478C=	NP_001300884.1:p.Arg160=
NM_004217.3:c.982C=	NP_004208.2:p.Arg328=
NR_132730.1:n.962C=
NR_132731.1:n.847C=
XM_011524070.1:c.886C=	XP_011522372.1:p.Arg296=
XM_011524072.1:c.859C=	XP_011522374.1:p.Arg287=
XR_934118.1:n.1191C=
NM_001313953.2:c.886C=	NP_001300882.1:p.Arg296=
XM_011524072.3:c.859C=	XP_011522374.1:p.Arg287=
XM_017025307.2:c.859C=	XP_016880796.1:p.Arg287=
XM_017025308.2:c.763C=	XP_016880797.1:p.Arg255=
XM_017025309.1:c.526C=	XP_016880798.1:p.Arg176=
XM_017025310.1:c.526C=	XP_016880799.1:p.Arg176=
XM_017025311.1:c.526C=	XP_016880800.1:p.Arg176=
NM_004217.4:c.982C= MANE Select	NP_004208.2:p.Arg328=
NM_001256834.3:c.859C=	NP_001243763.1:p.Arg287=
NM_001284526.2:c.985C=	NP_001271455.1:p.Arg329=
NM_001313950.2:c.982C=	NP_001300879.1:p.Arg328=
NM_001313952.2:c.862C=	NP_001300881.1:p.Arg288=
NM_001313953.3:c.886C=	NP_001300882.1:p.Arg296=
NM_001313954.2:c.526C=	NP_001300883.1:p.Arg176=
NM_001313955.2:c.478C=	NP_001300884.1:p.Arg160=
NR_132730.2:n.911C=