Canonical Allele Identifier: CA397985225

Gene: AURKB

Linked Data

• MyVariant Identifiers: chr17:g.8108244A>T (hg19) ; chr17:g.8204926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8204926A>T , CM000679.2:g.8204926A>T	GRCh38
NC_000017.10:g.8108244A>T , CM000679.1:g.8108244A>T	GRCh37
NC_000017.9:g.8048969A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000585124.6:c.980T>A MANE Select	ENSP00000463999.1:p.Val327Asp
ENST00000316199.10:c.983T>A	ENSP00000313950.6:p.Val328Asp
ENST00000534871.5:c.857T>A	ENSP00000443869.1:p.Val286Asp
ENST00000578549.5:c.884T>A	ENSP00000462207.1:p.Val295Asp
ENST00000580998.5:c.*327T>A	ENSP00000461981.1:n.*327T>A
ENST00000584972.5:c.672T>A
ENST00000585124.5:c.980T>A	ENSP00000463999.1:p.Val327Asp
NM_001256834.1:c.857T>A	NP_001243763.1:p.Val286Asp
NM_001256834.2:c.857T>A	NP_001243763.1:p.Val286Asp
NM_001284526.1:c.983T>A	NP_001271455.1:p.Val328Asp
NM_001313950.1:c.980T>A	NP_001300879.1:p.Val327Asp
NM_001313951.1:c.857T>A	NP_001300880.1:p.Val286Asp
NM_001313952.1:c.860T>A	NP_001300881.1:p.Val287Asp
NM_001313953.1:c.884T>A	NP_001300882.1:p.Val295Asp
NM_001313954.1:c.524T>A	NP_001300883.1:p.Val175Asp
NM_001313955.1:c.476T>A	NP_001300884.1:p.Val159Asp
NM_004217.3:c.980T>A	NP_004208.2:p.Val327Asp
NR_132730.1:n.960T>A
NR_132731.1:n.845T>A
XM_011524070.1:c.884T>A	XP_011522372.1:p.Val295Asp
XM_011524072.1:c.857T>A	XP_011522374.1:p.Val286Asp
XR_934118.1:n.1189T>A
NM_001313953.2:c.884T>A	NP_001300882.1:p.Val295Asp
XM_011524072.3:c.857T>A	XP_011522374.1:p.Val286Asp
XM_017025307.2:c.857T>A	XP_016880796.1:p.Val286Asp
XM_017025308.2:c.761T>A	XP_016880797.1:p.Val254Asp
XM_017025309.1:c.524T>A	XP_016880798.1:p.Val175Asp
XM_017025310.1:c.524T>A	XP_016880799.1:p.Val175Asp
XM_017025311.1:c.524T>A	XP_016880800.1:p.Val175Asp
NM_004217.4:c.980T>A MANE Select	NP_004208.2:p.Val327Asp
NM_001256834.3:c.857T>A	NP_001243763.1:p.Val286Asp
NM_001284526.2:c.983T>A	NP_001271455.1:p.Val328Asp
NM_001313950.2:c.980T>A	NP_001300879.1:p.Val327Asp
NM_001313952.2:c.860T>A	NP_001300881.1:p.Val287Asp
NM_001313953.3:c.884T>A	NP_001300882.1:p.Val295Asp
NM_001313954.2:c.524T>A	NP_001300883.1:p.Val175Asp
NM_001313955.2:c.476T>A	NP_001300884.1:p.Val159Asp
NR_132730.2:n.909T>A