Canonical Allele Identifier: CA2246210491

Gene: AURKB

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204934G= , CM000679.2:g.8204934G=	GRCh38
NC_000017.10:g.8108252G= , CM000679.1:g.8108252G=	GRCh37
NC_000017.9:g.8048977G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.972C= MANE Select	ENSP00000463999.1:p.His324=
ENST00000316199.10:c.975C=	ENSP00000313950.6:p.His325=
ENST00000534871.5:c.849C=	ENSP00000443869.1:p.His283=
ENST00000578549.5:c.876C=	ENSP00000462207.1:p.His292=
ENST00000580998.5:c.*319C=	ENSP00000461981.1:n.*319C=
ENST00000584972.5:c.664C=
ENST00000585124.5:c.972C=	ENSP00000463999.1:p.His324=
NM_001256834.1:c.849C=	NP_001243763.1:p.His283=
NM_001256834.2:c.849C=	NP_001243763.1:p.His283=
NM_001284526.1:c.975C=	NP_001271455.1:p.His325=
NM_001313950.1:c.972C=	NP_001300879.1:p.His324=
NM_001313951.1:c.849C=	NP_001300880.1:p.His283=
NM_001313952.1:c.852C=	NP_001300881.1:p.His284=
NM_001313953.1:c.876C=	NP_001300882.1:p.His292=
NM_001313954.1:c.516C=	NP_001300883.1:p.His172=
NM_001313955.1:c.468C=	NP_001300884.1:p.His156=
NM_004217.3:c.972C=	NP_004208.2:p.His324=
NR_132730.1:n.952C=
NR_132731.1:n.837C=
XM_011524070.1:c.876C=	XP_011522372.1:p.His292=
XM_011524072.1:c.849C=	XP_011522374.1:p.His283=
XR_934118.1:n.1181C=
NM_001313953.2:c.876C=	NP_001300882.1:p.His292=
XM_011524072.3:c.849C=	XP_011522374.1:p.His283=
XM_017025307.2:c.849C=	XP_016880796.1:p.His283=
XM_017025308.2:c.753C=	XP_016880797.1:p.His251=
XM_017025309.1:c.516C=	XP_016880798.1:p.His172=
XM_017025310.1:c.516C=	XP_016880799.1:p.His172=
XM_017025311.1:c.516C=	XP_016880800.1:p.His172=
NM_004217.4:c.972C= MANE Select	NP_004208.2:p.His324=
NM_001256834.3:c.849C=	NP_001243763.1:p.His283=
NM_001284526.2:c.975C=	NP_001271455.1:p.His325=
NM_001313950.2:c.972C=	NP_001300879.1:p.His324=
NM_001313952.2:c.852C=	NP_001300881.1:p.His284=
NM_001313953.3:c.876C=	NP_001300882.1:p.His292=
NM_001313954.2:c.516C=	NP_001300883.1:p.His172=
NM_001313955.2:c.468C=	NP_001300884.1:p.His156=
NR_132730.2:n.901C=