Canonical Allele Identifier: CA2612330551
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090007dup , CM000673.2:g.8090007dup GRCh38
NC_000011.9:g.8111554dup , CM000673.1:g.8111554dup GRCh37
NC_000011.8:g.8068130dup NCBI36
NG_029912.1:g.56375dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.91-62dup MANE Select ENSP00000299506.3:n.91-62dup
ENST00000299506.2:c.91-62dup ENSP00000299506.2:n.91-62dup
ENST00000305253.8:c.256-62dup ENSP00000305426.4:n.256-62dup
ENST00000534099.5:c.109-62dup ENSP00000434400.1:n.109-62dup
NM_003320.4:c.256-62dup NP_003311.2:n.256-62dup
NM_177972.2:c.91-62dup NP_813977.1:n.91-62dup
XM_005253109.2:c.217-62dup XP_005253166.1:n.217-62dup
XM_011520344.1:c.127-62dup XP_011518646.1:n.127-62dup
XM_005253109.3:c.217-62dup XP_005253166.1:n.217-62dup
XM_011520344.2:c.127-62dup XP_011518646.1:n.127-62dup
NM_177972.3:c.91-62dup MANE Select NP_813977.1:n.91-62dup
NM_003320.5:c.256-62dup NP_003311.2:n.256-62dup