Canonical Allele Identifier: CA379562831
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090141C>G , CM000673.2:g.8090141C>G GRCh38
NC_000011.9:g.8111688C>G , CM000673.1:g.8111688C>G GRCh37
NC_000011.8:g.8068264C>G NCBI36
NG_029912.1:g.56509C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.163C>G MANE Select ENSP00000299506.3:p.Arg55Gly
ENST00000299506.2:c.163C>G ENSP00000299506.2:p.Arg55Gly
ENST00000305253.8:c.328C>G ENSP00000305426.4:p.Arg110Gly
ENST00000534099.5:c.181C>G ENSP00000434400.1:p.Arg61Gly
NM_003320.4:c.328C>G NP_003311.2:p.Arg110Gly
NM_177972.2:c.163C>G NP_813977.1:p.Arg55Gly
XM_005253109.2:c.289C>G XP_005253166.1:p.Arg97Gly
XM_011520344.1:c.199C>G XP_011518646.1:p.Arg67Gly
XM_005253109.3:c.289C>G XP_005253166.1:p.Arg97Gly
XM_011520344.2:c.199C>G XP_011518646.1:p.Arg67Gly
NM_177972.3:c.163C>G MANE Select NP_813977.1:p.Arg55Gly
NM_003320.5:c.328C>G NP_003311.2:p.Arg110Gly