Canonical Allele Identifier: CA2246210489

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204931A= , CM000679.2:g.8204931A=	GRCh38
NC_000017.10:g.8108249A= , CM000679.1:g.8108249A=	GRCh37
NC_000017.9:g.8048974A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.975T= MANE Select	ENSP00000463999.1:p.Pro325=
ENST00000316199.10:c.978T=	ENSP00000313950.6:p.Pro326=
ENST00000534871.5:c.852T=	ENSP00000443869.1:p.Pro284=
ENST00000578549.5:c.879T=	ENSP00000462207.1:p.Pro293=
ENST00000580998.5:c.*322T=	ENSP00000461981.1:n.*322T=
ENST00000584972.5:c.667T=
ENST00000585124.5:c.975T=	ENSP00000463999.1:p.Pro325=
NM_001256834.1:c.852T=	NP_001243763.1:p.Pro284=
NM_001256834.2:c.852T=	NP_001243763.1:p.Pro284=
NM_001284526.1:c.978T=	NP_001271455.1:p.Pro326=
NM_001313950.1:c.975T=	NP_001300879.1:p.Pro325=
NM_001313951.1:c.852T=	NP_001300880.1:p.Pro284=
NM_001313952.1:c.855T=	NP_001300881.1:p.Pro285=
NM_001313953.1:c.879T=	NP_001300882.1:p.Pro293=
NM_001313954.1:c.519T=	NP_001300883.1:p.Pro173=
NM_001313955.1:c.471T=	NP_001300884.1:p.Pro157=
NM_004217.3:c.975T=	NP_004208.2:p.Pro325=
NR_132730.1:n.955T=
NR_132731.1:n.840T=
XM_011524070.1:c.879T=	XP_011522372.1:p.Pro293=
XM_011524072.1:c.852T=	XP_011522374.1:p.Pro284=
XR_934118.1:n.1184T=
NM_001313953.2:c.879T=	NP_001300882.1:p.Pro293=
XM_011524072.3:c.852T=	XP_011522374.1:p.Pro284=
XM_017025307.2:c.852T=	XP_016880796.1:p.Pro284=
XM_017025308.2:c.756T=	XP_016880797.1:p.Pro252=
XM_017025309.1:c.519T=	XP_016880798.1:p.Pro173=
XM_017025310.1:c.519T=	XP_016880799.1:p.Pro173=
XM_017025311.1:c.519T=	XP_016880800.1:p.Pro173=
NM_004217.4:c.975T= MANE Select	NP_004208.2:p.Pro325=
NM_001256834.3:c.852T=	NP_001243763.1:p.Pro284=
NM_001284526.2:c.978T=	NP_001271455.1:p.Pro326=
NM_001313950.2:c.975T=	NP_001300879.1:p.Pro325=
NM_001313952.2:c.855T=	NP_001300881.1:p.Pro285=
NM_001313953.3:c.879T=	NP_001300882.1:p.Pro293=
NM_001313954.2:c.519T=	NP_001300883.1:p.Pro173=
NM_001313955.2:c.471T=	NP_001300884.1:p.Pro157=
NR_132730.2:n.904T=