Canonical Allele Identifier: CA448708069
Gene: TUBB2A HGNC NCBI

Linked Data

COSMIC: COSM1443182
MyVariant Identifiers: chr6:g.3154851del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.3154620del , CM000668.2:g.3154620del GRCh38
NC_000006.11:g.3154854del , CM000668.1:g.3154854del GRCh37
NC_000006.10:g.3099853del NCBI36
NG_042223.1:g.7933del

Transcript Alleles

HGVS Amino-acid Change
ENST00000333628.4:c.584del MANE Select ENSP00000369703.2:p.Asn195ThrfsTer21
ENST00000679400.1:n.640del
ENST00000679907.1:n.972del
ENST00000680036.1:n.1366del
ENST00000680967.1:n.1674del
ENST00000333628.3:c.584del ENSP00000369703.2:p.Asn195ThrfsTer21
ENST00000489942.1:n.779del
NM_001069.2:c.584del NP_001060.1:p.Asn195ThrfsTer21
NM_001310315.1:c.329del NP_001297244.1:p.Asn110ThrfsTer21
NM_001069.3:c.584del MANE Select NP_001060.1:p.Asn195ThrfsTer21
NM_001310315.2:c.329del NP_001297244.1:p.Asn110ThrfsTer21
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