Canonical Allele Identifier: CA2612330437
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8089806-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089809del , CM000673.2:g.8089809del GRCh38
NC_000011.9:g.8111356del , CM000673.1:g.8111356del GRCh37
NC_000011.8:g.8067932del NCBI36
NG_029912.1:g.56177del

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.90+148del MANE Select ENSP00000299506.3:n.90+148del
ENST00000299506.2:c.90+148del ENSP00000299506.2:n.90+148del
ENST00000305253.8:c.255+148del ENSP00000305426.4:n.255+148del
ENST00000534099.5:c.108+148del ENSP00000434400.1:n.108+148del
NM_003320.4:c.255+148del NP_003311.2:n.255+148del
NM_177972.2:c.90+148del NP_813977.1:n.90+148del
XM_005253109.2:c.216+148del XP_005253166.1:n.216+148del
XM_011520344.1:c.126+148del XP_011518646.1:n.126+148del
XM_005253109.3:c.216+148del XP_005253166.1:n.216+148del
XM_011520344.2:c.126+148del XP_011518646.1:n.126+148del
NM_177972.3:c.90+148del MANE Select NP_813977.1:n.90+148del
NM_003320.5:c.255+148del NP_003311.2:n.255+148del
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