Canonical Allele Identifier: CA379562276
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089620G>T , CM000673.2:g.8089620G>T GRCh38
NC_000011.9:g.8111167G>T , CM000673.1:g.8111167G>T GRCh37
NC_000011.8:g.8067743G>T NCBI36
NG_029912.1:g.55988G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.49G>T MANE Select ENSP00000299506.3:p.Asp17Tyr
ENST00000299506.2:c.49G>T ENSP00000299506.2:p.Asp17Tyr
ENST00000305253.8:c.214G>T ENSP00000305426.4:p.Asp72Tyr
ENST00000534099.5:c.67G>T ENSP00000434400.1:p.Asp23Tyr
NM_003320.4:c.214G>T NP_003311.2:p.Asp72Tyr
NM_177972.2:c.49G>T NP_813977.1:p.Asp17Tyr
XM_005253109.2:c.175G>T XP_005253166.1:p.Asp59Tyr
XM_011520344.1:c.85G>T XP_011518646.1:p.Asp29Tyr
XM_005253109.3:c.175G>T XP_005253166.1:p.Asp59Tyr
XM_011520344.2:c.85G>T XP_011518646.1:p.Asp29Tyr
NM_177972.3:c.49G>T MANE Select NP_813977.1:p.Asp17Tyr
NM_003320.5:c.214G>T NP_003311.2:p.Asp72Tyr