Canonical Allele Identifier: CA379562720
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090115T>A , CM000673.2:g.8090115T>A GRCh38
NC_000011.9:g.8111662T>A , CM000673.1:g.8111662T>A GRCh37
NC_000011.8:g.8068238T>A NCBI36
NG_029912.1:g.56483T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.137T>A MANE Select ENSP00000299506.3:p.Leu46Gln
ENST00000299506.2:c.137T>A ENSP00000299506.2:p.Leu46Gln
ENST00000305253.8:c.302T>A ENSP00000305426.4:p.Leu101Gln
ENST00000534099.5:c.155T>A ENSP00000434400.1:p.Leu52Gln
NM_003320.4:c.302T>A NP_003311.2:p.Leu101Gln
NM_177972.2:c.137T>A NP_813977.1:p.Leu46Gln
XM_005253109.2:c.263T>A XP_005253166.1:p.Leu88Gln
XM_011520344.1:c.173T>A XP_011518646.1:p.Leu58Gln
XM_005253109.3:c.263T>A XP_005253166.1:p.Leu88Gln
XM_011520344.2:c.173T>A XP_011518646.1:p.Leu58Gln
NM_177972.3:c.137T>A MANE Select NP_813977.1:p.Leu46Gln
NM_003320.5:c.302T>A NP_003311.2:p.Leu101Gln