Canonical Allele Identifier: CA379562237
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089610T>G , CM000673.2:g.8089610T>G GRCh38
NC_000011.9:g.8111157T>G , CM000673.1:g.8111157T>G GRCh37
NC_000011.8:g.8067733T>G NCBI36
NG_029912.1:g.55978T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39T>G MANE Select ENSP00000299506.3:p.Ser13Arg
ENST00000299506.2:c.39T>G ENSP00000299506.2:p.Ser13Arg
ENST00000305253.8:c.204T>G ENSP00000305426.4:p.Arg68=
ENST00000534099.5:c.57T>G ENSP00000434400.1:p.Ser19Arg
NM_003320.4:c.204T>G NP_003311.2:p.Arg68=
NM_177972.2:c.39T>G NP_813977.1:p.Ser13Arg
XM_005253109.2:c.165T>G XP_005253166.1:p.Ser55Arg
XM_011520344.1:c.75T>G XP_011518646.1:p.Ser25Arg
XM_005253109.3:c.165T>G XP_005253166.1:p.Ser55Arg
XM_011520344.2:c.75T>G XP_011518646.1:p.Ser25Arg
NM_177972.3:c.39T>G MANE Select NP_813977.1:p.Ser13Arg
NM_003320.5:c.204T>G NP_003311.2:p.Arg68=