Canonical Allele Identifier: CA934888042
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1808102924

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089487dup , CM000673.2:g.8089487dup GRCh38
NC_000011.9:g.8111034dup , CM000673.1:g.8111034dup GRCh37
NC_000011.8:g.8067610dup NCBI36
NG_029912.1:g.55855dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-123dup MANE Select ENSP00000299506.3:n.39-123dup
ENST00000299506.2:c.39-123dup ENSP00000299506.2:n.39-123dup
ENST00000305253.8:c.204-123dup ENSP00000305426.4:n.204-123dup
ENST00000534099.5:c.57-123dup ENSP00000434400.1:n.57-123dup
NM_003320.4:c.204-123dup NP_003311.2:n.204-123dup
NM_177972.2:c.39-123dup NP_813977.1:n.39-123dup
XM_005253109.2:c.165-123dup XP_005253166.1:n.165-123dup
XM_011520344.1:c.75-123dup XP_011518646.1:n.75-123dup
XM_005253109.3:c.165-123dup XP_005253166.1:n.165-123dup
XM_011520344.2:c.75-123dup XP_011518646.1:n.75-123dup
NM_177972.3:c.39-123dup MANE Select NP_813977.1:n.39-123dup
NM_003320.5:c.204-123dup NP_003311.2:n.204-123dup