Canonical Allele Identifier: CA379562822
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.160G>T MANE Select ENSP00000299506.3:p.Gly54Trp
ENST00000299506.2:c.160G>T ENSP00000299506.2:p.Gly54Trp
ENST00000305253.8:c.325G>T ENSP00000305426.4:p.Gly109Trp
ENST00000534099.5:c.178G>T ENSP00000434400.1:p.Gly60Trp
NM_003320.4:c.325G>T NP_003311.2:p.Gly109Trp
NM_177972.2:c.160G>T NP_813977.1:p.Gly54Trp
XM_005253109.2:c.286G>T XP_005253166.1:p.Gly96Trp
XM_011520344.1:c.196G>T XP_011518646.1:p.Gly66Trp
XM_005253109.3:c.286G>T XP_005253166.1:p.Gly96Trp
XM_011520344.2:c.196G>T XP_011518646.1:p.Gly66Trp
NM_177972.3:c.160G>T MANE Select NP_813977.1:p.Gly54Trp
NM_003320.5:c.325G>T NP_003311.2:p.Gly109Trp