Canonical Allele Identifier: CA665795620

Gene: TUBB8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.47971del , CM000672.2:g.47971del	GRCh38
NC_000010.10:g.93911del , CM000672.1:g.93911del	GRCh37
NC_000010.9:g.83911del	NCBI36
NG_046777.1:g.33490del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000568584.6:c.426del MANE Select	ENSP00000456206.2:p.Thr143LeufsTer22
ENST00000561967.1:c.*89del	ENSP00000454878.1:n.*89del
ENST00000562809.1:c.*89del	ENSP00000456899.1:n.*89del
ENST00000563456.1:n.535del
ENST00000564130.2:c.324del	ENSP00000457610.1:p.Thr109LeufsTer22
ENST00000567466.1:c.*270del	ENSP00000454914.1:n.*270del
ENST00000568584.5:c.426del	ENSP00000456206.1:p.Thr143LeufsTer22
ENST00000568866.5:c.315del	ENSP00000457062.1:p.Thr106LeufsTer22
NM_177987.2:c.426del	NP_817124.1:p.Thr143LeufsTer22
XM_011519458.1:c.210del	XP_011517760.1:p.Thr71LeufsTer22
XM_011519459.1:c.210del	XP_011517761.1:p.Thr71LeufsTer22
XM_011519460.1:c.64-97del	XP_011517762.1:n.64-97del
XM_011519459.3:c.210del	XP_011517761.1:p.Thr71LeufsTer22
XM_011519460.2:c.64-97del	XP_011517762.1:n.64-97del
XM_017016192.2:c.90del	XP_016871681.1:p.Thr31LeufsTer22
XM_017016193.2:c.90del	XP_016871682.1:p.Thr31LeufsTer22
NM_177987.3:c.426del MANE Select	NP_817124.1:p.Thr143LeufsTer22
NM_001389618.1:c.210del	NP_001376547.1:p.Thr71LeufsTer22
NM_001389619.1:c.210del	NP_001376548.1:p.Thr71LeufsTer22