Canonical Allele Identifier: CA379562965
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090174G>T , CM000673.2:g.8090174G>T GRCh38
NC_000011.9:g.8111721G>T , CM000673.1:g.8111721G>T GRCh37
NC_000011.8:g.8068297G>T NCBI36
NG_029912.1:g.56542G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.196G>T MANE Select ENSP00000299506.3:p.Glu66Ter
ENST00000299506.2:c.196G>T ENSP00000299506.2:p.Glu66Ter
ENST00000305253.8:c.361G>T ENSP00000305426.4:p.Glu121Ter
ENST00000534099.5:c.214G>T ENSP00000434400.1:p.Glu72Ter
NM_003320.4:c.361G>T NP_003311.2:p.Glu121Ter
NM_177972.2:c.196G>T NP_813977.1:p.Glu66Ter
XM_005253109.2:c.322G>T XP_005253166.1:p.Glu108Ter
XM_011520344.1:c.232G>T XP_011518646.1:p.Glu78Ter
XM_005253109.3:c.322G>T XP_005253166.1:p.Glu108Ter
XM_011520344.2:c.232G>T XP_011518646.1:p.Glu78Ter
NM_177972.3:c.196G>T MANE Select NP_813977.1:p.Glu66Ter
NM_003320.5:c.361G>T NP_003311.2:p.Glu121Ter