Canonical Allele Identifier: CA379562803
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090135G>A , CM000673.2:g.8090135G>A GRCh38
NC_000011.9:g.8111682G>A , CM000673.1:g.8111682G>A GRCh37
NC_000011.8:g.8068258G>A NCBI36
NG_029912.1:g.56503G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.157G>A MANE Select ENSP00000299506.3:p.Asp53Asn
ENST00000299506.2:c.157G>A ENSP00000299506.2:p.Asp53Asn
ENST00000305253.8:c.322G>A ENSP00000305426.4:p.Asp108Asn
ENST00000534099.5:c.175G>A ENSP00000434400.1:p.Asp59Asn
NM_003320.4:c.322G>A NP_003311.2:p.Asp108Asn
NM_177972.2:c.157G>A NP_813977.1:p.Asp53Asn
XM_005253109.2:c.283G>A XP_005253166.1:p.Asp95Asn
XM_011520344.1:c.193G>A XP_011518646.1:p.Asp65Asn
XM_005253109.3:c.283G>A XP_005253166.1:p.Asp95Asn
XM_011520344.2:c.193G>A XP_011518646.1:p.Asp65Asn
NM_177972.3:c.157G>A MANE Select NP_813977.1:p.Asp53Asn
NM_003320.5:c.322G>A NP_003311.2:p.Asp108Asn