Canonical Allele Identifier: CA597441538
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1564916930
MyVariant Identifiers: chr11:g.8111567del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090020del , CM000673.2:g.8090020del GRCh38
NC_000011.9:g.8111567del , CM000673.1:g.8111567del GRCh37
NC_000011.8:g.8068143del NCBI36
NG_029912.1:g.56388del

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-49del MANE Select ENSP00000299506.3:n.91-49del
ENST00000299506.2:c.91-49del ENSP00000299506.2:n.91-49del
ENST00000305253.8:c.256-49del ENSP00000305426.4:n.256-49del
ENST00000534099.5:c.109-49del ENSP00000434400.1:n.109-49del
NM_003320.4:c.256-49del NP_003311.2:n.256-49del
NM_177972.2:c.91-49del NP_813977.1:n.91-49del
XM_005253109.2:c.217-49del XP_005253166.1:n.217-49del
XM_011520344.1:c.127-49del XP_011518646.1:n.127-49del
XM_005253109.3:c.217-49del XP_005253166.1:n.217-49del
XM_011520344.2:c.127-49del XP_011518646.1:n.127-49del
NM_177972.3:c.91-49del MANE Select NP_813977.1:n.91-49del
NM_003320.5:c.256-49del NP_003311.2:n.256-49del