Canonical Allele Identifier: CA497768683

Gene: AURKB

Linked Data

• MyVariant Identifiers: chr17:g.8108336C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.8205018C>T , CM000679.2:g.8205018C>T	GRCh38
NC_000017.10:g.8108336C>T , CM000679.1:g.8108336C>T	GRCh37
NC_000017.9:g.8049061C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585124.6:c.888G>A MANE Select	ENSP00000463999.1:p.Val296=
ENST00000316199.10:c.891G>A	ENSP00000313950.6:p.Val297=
ENST00000534871.5:c.765G>A	ENSP00000443869.1:p.Val255=
ENST00000578549.5:c.792G>A	ENSP00000462207.1:p.Val264=
ENST00000578753.1:n.410G>A
ENST00000580998.5:c.*235G>A	ENSP00000461981.1:n.*235G>A
ENST00000584972.5:c.580G>A
ENST00000585124.5:c.888G>A	ENSP00000463999.1:p.Val296=
NM_001256834.1:c.765G>A	NP_001243763.1:p.Val255=
NM_001256834.2:c.765G>A	NP_001243763.1:p.Val255=
NM_001284526.1:c.891G>A	NP_001271455.1:p.Val297=
NM_001313950.1:c.888G>A	NP_001300879.1:p.Val296=
NM_001313951.1:c.765G>A	NP_001300880.1:p.Val255=
NM_001313952.1:c.768G>A	NP_001300881.1:p.Val256=
NM_001313953.1:c.792G>A	NP_001300882.1:p.Val264=
NM_001313954.1:c.432G>A	NP_001300883.1:p.Val144=
NM_001313955.1:c.384G>A	NP_001300884.1:p.Val128=
NM_004217.3:c.888G>A	NP_004208.2:p.Val296=
NR_132730.1:n.868G>A
NR_132731.1:n.753G>A
XM_011524070.1:c.792G>A	XP_011522372.1:p.Val264=
XM_011524072.1:c.765G>A	XP_011522374.1:p.Val255=
XR_934118.1:n.1097G>A
NM_001313953.2:c.792G>A	NP_001300882.1:p.Val264=
XM_011524072.3:c.765G>A	XP_011522374.1:p.Val255=
XM_017025307.2:c.765G>A	XP_016880796.1:p.Val255=
XM_017025308.2:c.669G>A	XP_016880797.1:p.Val223=
XM_017025309.1:c.432G>A	XP_016880798.1:p.Val144=
XM_017025310.1:c.432G>A	XP_016880799.1:p.Val144=
XM_017025311.1:c.432G>A	XP_016880800.1:p.Val144=
NM_004217.4:c.888G>A MANE Select	NP_004208.2:p.Val296=
NM_001256834.3:c.765G>A	NP_001243763.1:p.Val255=
NM_001284526.2:c.891G>A	NP_001271455.1:p.Val297=
NM_001313950.2:c.888G>A	NP_001300879.1:p.Val296=
NM_001313952.2:c.768G>A	NP_001300881.1:p.Val256=
NM_001313953.3:c.792G>A	NP_001300882.1:p.Val264=
NM_001313954.2:c.432G>A	NP_001300883.1:p.Val144=
NM_001313955.2:c.384G>A	NP_001300884.1:p.Val128=
NR_132730.2:n.817G>A