Canonical Allele Identifier: CA379562406
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089648A>T , CM000673.2:g.8089648A>T GRCh38
NC_000011.9:g.8111195A>T , CM000673.1:g.8111195A>T GRCh37
NC_000011.8:g.8067771A>T NCBI36
NG_029912.1:g.56016A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.77A>T MANE Select ENSP00000299506.3:p.Lys26Met
ENST00000299506.2:c.77A>T ENSP00000299506.2:p.Lys26Met
ENST00000305253.8:c.242A>T ENSP00000305426.4:p.Lys81Met
ENST00000534099.5:c.95A>T ENSP00000434400.1:p.Lys32Met
NM_003320.4:c.242A>T NP_003311.2:p.Lys81Met
NM_177972.2:c.77A>T NP_813977.1:p.Lys26Met
XM_005253109.2:c.203A>T XP_005253166.1:p.Lys68Met
XM_011520344.1:c.113A>T XP_011518646.1:p.Lys38Met
XM_005253109.3:c.203A>T XP_005253166.1:p.Lys68Met
XM_011520344.2:c.113A>T XP_011518646.1:p.Lys38Met
NM_177972.3:c.77A>T MANE Select NP_813977.1:p.Lys26Met
NM_003320.5:c.242A>T NP_003311.2:p.Lys81Met