Canonical Allele Identifier: CA379562630
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090093A>T , CM000673.2:g.8090093A>T GRCh38
NC_000011.9:g.8111640A>T , CM000673.1:g.8111640A>T GRCh37
NC_000011.8:g.8068216A>T NCBI36
NG_029912.1:g.56461A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.115A>T MANE Select ENSP00000299506.3:p.Lys39Ter
ENST00000299506.2:c.115A>T ENSP00000299506.2:p.Lys39Ter
ENST00000305253.8:c.280A>T ENSP00000305426.4:p.Lys94Ter
ENST00000534099.5:c.133A>T ENSP00000434400.1:p.Lys45Ter
NM_003320.4:c.280A>T NP_003311.2:p.Lys94Ter
NM_177972.2:c.115A>T NP_813977.1:p.Lys39Ter
XM_005253109.2:c.241A>T XP_005253166.1:p.Lys81Ter
XM_011520344.1:c.151A>T XP_011518646.1:p.Lys51Ter
XM_005253109.3:c.241A>T XP_005253166.1:p.Lys81Ter
XM_011520344.2:c.151A>T XP_011518646.1:p.Lys51Ter
NM_177972.3:c.115A>T MANE Select NP_813977.1:p.Lys39Ter
NM_003320.5:c.280A>T NP_003311.2:p.Lys94Ter