Canonical Allele Identifier: CA379562661
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8090099-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090099A>T , CM000673.2:g.8090099A>T GRCh38
NC_000011.9:g.8111646A>T , CM000673.1:g.8111646A>T GRCh37
NC_000011.8:g.8068222A>T NCBI36
NG_029912.1:g.56467A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.121A>T MANE Select ENSP00000299506.3:p.Lys41Ter
ENST00000299506.2:c.121A>T ENSP00000299506.2:p.Lys41Ter
ENST00000305253.8:c.286A>T ENSP00000305426.4:p.Lys96Ter
ENST00000534099.5:c.139A>T ENSP00000434400.1:p.Lys47Ter
NM_003320.4:c.286A>T NP_003311.2:p.Lys96Ter
NM_177972.2:c.121A>T NP_813977.1:p.Lys41Ter
XM_005253109.2:c.247A>T XP_005253166.1:p.Lys83Ter
XM_011520344.1:c.157A>T XP_011518646.1:p.Lys53Ter
XM_005253109.3:c.247A>T XP_005253166.1:p.Lys83Ter
XM_011520344.2:c.157A>T XP_011518646.1:p.Lys53Ter
NM_177972.3:c.121A>T MANE Select NP_813977.1:p.Lys41Ter
NM_003320.5:c.286A>T NP_003311.2:p.Lys96Ter