Canonical Allele Identifier: CA379562320
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089629A>T , CM000673.2:g.8089629A>T GRCh38
NC_000011.9:g.8111176A>T , CM000673.1:g.8111176A>T GRCh37
NC_000011.8:g.8067752A>T NCBI36
NG_029912.1:g.55997A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.58A>T MANE Select ENSP00000299506.3:p.Arg20Ter
ENST00000299506.2:c.58A>T ENSP00000299506.2:p.Arg20Ter
ENST00000305253.8:c.223A>T ENSP00000305426.4:p.Arg75Ter
ENST00000534099.5:c.76A>T ENSP00000434400.1:p.Arg26Ter
NM_003320.4:c.223A>T NP_003311.2:p.Arg75Ter
NM_177972.2:c.58A>T NP_813977.1:p.Arg20Ter
XM_005253109.2:c.184A>T XP_005253166.1:p.Arg62Ter
XM_011520344.1:c.94A>T XP_011518646.1:p.Arg32Ter
XM_005253109.3:c.184A>T XP_005253166.1:p.Arg62Ter
XM_011520344.2:c.94A>T XP_011518646.1:p.Arg32Ter
NM_177972.3:c.58A>T MANE Select NP_813977.1:p.Arg20Ter
NM_003320.5:c.223A>T NP_003311.2:p.Arg75Ter