Canonical Allele Identifier: CA379562640
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090096A>T , CM000673.2:g.8090096A>T GRCh38
NC_000011.9:g.8111643A>T , CM000673.1:g.8111643A>T GRCh37
NC_000011.8:g.8068219A>T NCBI36
NG_029912.1:g.56464A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.118A>T MANE Select ENSP00000299506.3:p.Lys40Ter
ENST00000299506.2:c.118A>T ENSP00000299506.2:p.Lys40Ter
ENST00000305253.8:c.283A>T ENSP00000305426.4:p.Lys95Ter
ENST00000534099.5:c.136A>T ENSP00000434400.1:p.Lys46Ter
NM_003320.4:c.283A>T NP_003311.2:p.Lys95Ter
NM_177972.2:c.118A>T NP_813977.1:p.Lys40Ter
XM_005253109.2:c.244A>T XP_005253166.1:p.Lys82Ter
XM_011520344.1:c.154A>T XP_011518646.1:p.Lys52Ter
XM_005253109.3:c.244A>T XP_005253166.1:p.Lys82Ter
XM_011520344.2:c.154A>T XP_011518646.1:p.Lys52Ter
NM_177972.3:c.118A>T MANE Select NP_813977.1:p.Lys40Ter
NM_003320.5:c.283A>T NP_003311.2:p.Lys95Ter