Canonical Allele Identifier: CA379562818
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8090138-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090138G>A , CM000673.2:g.8090138G>A GRCh38
NC_000011.9:g.8111685G>A , CM000673.1:g.8111685G>A GRCh37
NC_000011.8:g.8068261G>A NCBI36
NG_029912.1:g.56506G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.160G>A MANE Select ENSP00000299506.3:p.Gly54Arg
ENST00000299506.2:c.160G>A ENSP00000299506.2:p.Gly54Arg
ENST00000305253.8:c.325G>A ENSP00000305426.4:p.Gly109Arg
ENST00000534099.5:c.178G>A ENSP00000434400.1:p.Gly60Arg
NM_003320.4:c.325G>A NP_003311.2:p.Gly109Arg
NM_177972.2:c.160G>A NP_813977.1:p.Gly54Arg
XM_005253109.2:c.286G>A XP_005253166.1:p.Gly96Arg
XM_011520344.1:c.196G>A XP_011518646.1:p.Gly66Arg
XM_005253109.3:c.286G>A XP_005253166.1:p.Gly96Arg
XM_011520344.2:c.196G>A XP_011518646.1:p.Gly66Arg
NM_177972.3:c.160G>A MANE Select NP_813977.1:p.Gly54Arg
NM_003320.5:c.325G>A NP_003311.2:p.Gly109Arg