Canonical Allele Identifier: CA379563023
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090187T>C , CM000673.2:g.8090187T>C GRCh38
NC_000011.9:g.8111734T>C , CM000673.1:g.8111734T>C GRCh37
NC_000011.8:g.8068310T>C NCBI36
NG_029912.1:g.56555T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.209T>C MANE Select ENSP00000299506.3:p.Leu70Pro
ENST00000299506.2:c.209T>C ENSP00000299506.2:p.Leu70Pro
ENST00000305253.8:c.374T>C ENSP00000305426.4:p.Leu125Pro
ENST00000534099.5:c.227T>C ENSP00000434400.1:p.Leu76Pro
NM_003320.4:c.374T>C NP_003311.2:p.Leu125Pro
NM_177972.2:c.209T>C NP_813977.1:p.Leu70Pro
XM_005253109.2:c.335T>C XP_005253166.1:p.Leu112Pro
XM_011520344.1:c.245T>C XP_011518646.1:p.Leu82Pro
XM_005253109.3:c.335T>C XP_005253166.1:p.Leu112Pro
XM_011520344.2:c.245T>C XP_011518646.1:p.Leu82Pro
NM_177972.3:c.209T>C MANE Select NP_813977.1:p.Leu70Pro
NM_003320.5:c.374T>C NP_003311.2:p.Leu125Pro