Canonical Allele Identifier: CA379562899
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090160C>A , CM000673.2:g.8090160C>A GRCh38
NC_000011.9:g.8111707C>A , CM000673.1:g.8111707C>A GRCh37
NC_000011.8:g.8068283C>A NCBI36
NG_029912.1:g.56528C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.182C>A MANE Select ENSP00000299506.3:p.Ala61Asp
ENST00000299506.2:c.182C>A ENSP00000299506.2:p.Ala61Asp
ENST00000305253.8:c.347C>A ENSP00000305426.4:p.Ala116Asp
ENST00000534099.5:c.200C>A ENSP00000434400.1:p.Ala67Asp
NM_003320.4:c.347C>A NP_003311.2:p.Ala116Asp
NM_177972.2:c.182C>A NP_813977.1:p.Ala61Asp
XM_005253109.2:c.308C>A XP_005253166.1:p.Ala103Asp
XM_011520344.1:c.218C>A XP_011518646.1:p.Ala73Asp
XM_005253109.3:c.308C>A XP_005253166.1:p.Ala103Asp
XM_011520344.2:c.218C>A XP_011518646.1:p.Ala73Asp
NM_177972.3:c.182C>A MANE Select NP_813977.1:p.Ala61Asp
NM_003320.5:c.347C>A NP_003311.2:p.Ala116Asp