Canonical Allele Identifier: CA2741147967
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090105del , CM000673.2:g.8090105del GRCh38
NC_000011.9:g.8111652del , CM000673.1:g.8111652del GRCh37
NC_000011.8:g.8068228del NCBI36
NG_029912.1:g.56473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.127del MANE Select ENSP00000299506.3:p.Gln43ArgfsTer4
ENST00000299506.2:c.127del ENSP00000299506.2:p.Gln43ArgfsTer4
ENST00000305253.8:c.292del ENSP00000305426.4:p.Gln98ArgfsTer4
ENST00000534099.5:c.145del ENSP00000434400.1:p.Gln49ArgfsTer4
NM_003320.4:c.292del NP_003311.2:p.Gln98ArgfsTer4
NM_177972.2:c.127del NP_813977.1:p.Gln43ArgfsTer4
XM_005253109.2:c.253del XP_005253166.1:p.Gln85ArgfsTer4
XM_011520344.1:c.163del XP_011518646.1:p.Gln55ArgfsTer4
XM_005253109.3:c.253del XP_005253166.1:p.Gln85ArgfsTer4
XM_011520344.2:c.163del XP_011518646.1:p.Gln55ArgfsTer4
NM_177972.3:c.127del MANE Select NP_813977.1:p.Gln43ArgfsTer4
NM_003320.5:c.292del NP_003311.2:p.Gln98ArgfsTer4