Canonical Allele Identifier: CA8371309

Gene: AURKB

Linked Data

• dbSNP Id: rs369229594
• ExAC: 17:8108242 G / A
• gnomAD v2: 17-8108242-G-A
• gnomAD v3: 17-8204924-G-A
• gnomAD v4: 17-8204924-G-A
• MyVariant Identifiers: chr17:g.8108242G>A (hg19) ; chr17:g.8204924G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000585124.6:c.982C>T MANE Select	ENSP00000463999.1:p.Arg328Trp
ENST00000316199.10:c.985C>T	ENSP00000313950.6:p.Arg329Trp
ENST00000534871.5:c.859C>T	ENSP00000443869.1:p.Arg287Trp
ENST00000578549.5:c.886C>T	ENSP00000462207.1:p.Arg296Trp
ENST00000580998.5:c.*329C>T	ENSP00000461981.1:n.*329C>T
ENST00000584972.5:c.674C>T
ENST00000585124.5:c.982C>T	ENSP00000463999.1:p.Arg328Trp
NM_001256834.1:c.859C>T	NP_001243763.1:p.Arg287Trp
NM_001256834.2:c.859C>T	NP_001243763.1:p.Arg287Trp
NM_001284526.1:c.985C>T	NP_001271455.1:p.Arg329Trp
NM_001313950.1:c.982C>T	NP_001300879.1:p.Arg328Trp
NM_001313951.1:c.859C>T	NP_001300880.1:p.Arg287Trp
NM_001313952.1:c.862C>T	NP_001300881.1:p.Arg288Trp
NM_001313953.1:c.886C>T	NP_001300882.1:p.Arg296Trp
NM_001313954.1:c.526C>T	NP_001300883.1:p.Arg176Trp
NM_001313955.1:c.478C>T	NP_001300884.1:p.Arg160Trp
NM_004217.3:c.982C>T	NP_004208.2:p.Arg328Trp
NR_132730.1:n.962C>T
NR_132731.1:n.847C>T
XM_011524070.1:c.886C>T	XP_011522372.1:p.Arg296Trp
XM_011524072.1:c.859C>T	XP_011522374.1:p.Arg287Trp
XR_934118.1:n.1191C>T
NM_001313953.2:c.886C>T	NP_001300882.1:p.Arg296Trp
XM_011524072.3:c.859C>T	XP_011522374.1:p.Arg287Trp
XM_017025307.2:c.859C>T	XP_016880796.1:p.Arg287Trp
XM_017025308.2:c.763C>T	XP_016880797.1:p.Arg255Trp
XM_017025309.1:c.526C>T	XP_016880798.1:p.Arg176Trp
XM_017025310.1:c.526C>T	XP_016880799.1:p.Arg176Trp
XM_017025311.1:c.526C>T	XP_016880800.1:p.Arg176Trp
NM_004217.4:c.982C>T MANE Select	NP_004208.2:p.Arg328Trp
NM_001256834.3:c.859C>T	NP_001243763.1:p.Arg287Trp
NM_001284526.2:c.985C>T	NP_001271455.1:p.Arg329Trp
NM_001313950.2:c.982C>T	NP_001300879.1:p.Arg328Trp
NM_001313952.2:c.862C>T	NP_001300881.1:p.Arg288Trp
NM_001313953.3:c.886C>T	NP_001300882.1:p.Arg296Trp
NM_001313954.2:c.526C>T	NP_001300883.1:p.Arg176Trp
NM_001313955.2:c.478C>T	NP_001300884.1:p.Arg160Trp
NR_132730.2:n.911C>T