Canonical Allele Identifier: CA217414791
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs926429464

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089385_8089386del , CM000673.2:g.8089385_8089386del GRCh38
NC_000011.9:g.8110932_8110933del , CM000673.1:g.8110932_8110933del GRCh37
NC_000011.8:g.8067508_8067509del NCBI36
NG_029912.1:g.55753_55754del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-225_39-224del MANE Select ENSP00000299506.3:n.39-225_39-224del
ENST00000299506.2:c.39-225_39-224del ENSP00000299506.2:n.39-225_39-224del
ENST00000305253.8:c.204-225_204-224del ENSP00000305426.4:n.204-225_204-224del
ENST00000534099.5:c.57-225_57-224del ENSP00000434400.1:n.57-225_57-224del
NM_003320.4:c.204-225_204-224del NP_003311.2:n.204-225_204-224del
NM_177972.2:c.39-225_39-224del NP_813977.1:n.39-225_39-224del
XM_005253109.2:c.165-225_165-224del XP_005253166.1:n.165-225_165-224del
XM_011520344.1:c.75-225_75-224del XP_011518646.1:n.75-225_75-224del
XM_005253109.3:c.165-225_165-224del XP_005253166.1:n.165-225_165-224del
XM_011520344.2:c.75-225_75-224del XP_011518646.1:n.75-225_75-224del
NM_177972.3:c.39-225_39-224del MANE Select NP_813977.1:n.39-225_39-224del
NM_003320.5:c.204-225_204-224del NP_003311.2:n.204-225_204-224del