Canonical Allele Identifier: CA379562550
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090073C>G , CM000673.2:g.8090073C>G GRCh38
NC_000011.9:g.8111620C>G , CM000673.1:g.8111620C>G GRCh37
NC_000011.8:g.8068196C>G NCBI36
NG_029912.1:g.56441C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.95C>G MANE Select ENSP00000299506.3:p.Ala32Gly
ENST00000299506.2:c.95C>G ENSP00000299506.2:p.Ala32Gly
ENST00000305253.8:c.260C>G ENSP00000305426.4:p.Ala87Gly
ENST00000534099.5:c.113C>G ENSP00000434400.1:p.Ala38Gly
NM_003320.4:c.260C>G NP_003311.2:p.Ala87Gly
NM_177972.2:c.95C>G NP_813977.1:p.Ala32Gly
XM_005253109.2:c.221C>G XP_005253166.1:p.Ala74Gly
XM_011520344.1:c.131C>G XP_011518646.1:p.Ala44Gly
XM_005253109.3:c.221C>G XP_005253166.1:p.Ala74Gly
XM_011520344.2:c.131C>G XP_011518646.1:p.Ala44Gly
NM_177972.3:c.95C>G MANE Select NP_813977.1:p.Ala32Gly
NM_003320.5:c.260C>G NP_003311.2:p.Ala87Gly