Canonical Allele Identifier: CA379562592
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090084C>T , CM000673.2:g.8090084C>T GRCh38
NC_000011.9:g.8111631C>T , CM000673.1:g.8111631C>T GRCh37
NC_000011.8:g.8068207C>T NCBI36
NG_029912.1:g.56452C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.106C>T MANE Select ENSP00000299506.3:p.Gln36Ter
ENST00000299506.2:c.106C>T ENSP00000299506.2:p.Gln36Ter
ENST00000305253.8:c.271C>T ENSP00000305426.4:p.Gln91Ter
ENST00000534099.5:c.124C>T ENSP00000434400.1:p.Gln42Ter
NM_003320.4:c.271C>T NP_003311.2:p.Gln91Ter
NM_177972.2:c.106C>T NP_813977.1:p.Gln36Ter
XM_005253109.2:c.232C>T XP_005253166.1:p.Gln78Ter
XM_011520344.1:c.142C>T XP_011518646.1:p.Gln48Ter
XM_005253109.3:c.232C>T XP_005253166.1:p.Gln78Ter
XM_011520344.2:c.142C>T XP_011518646.1:p.Gln48Ter
NM_177972.3:c.106C>T MANE Select NP_813977.1:p.Gln36Ter
NM_003320.5:c.271C>T NP_003311.2:p.Gln91Ter