Canonical Allele Identifier: CA2790351853
Gene: TUB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089846_8089847insAC , CM000673.2:g.8089846_8089847insAC GRCh38
NC_000011.9:g.8111393_8111394insAC , CM000673.1:g.8111393_8111394insAC GRCh37
NC_000011.8:g.8067969_8067970insAC NCBI36
NG_029912.1:g.56214_56215insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.90+185_90+186insAC MANE Select ENSP00000299506.3:n.90+185_90+186insAC
ENST00000299506.2:c.90+185_90+186insAC ENSP00000299506.2:n.90+185_90+186insAC
ENST00000305253.8:c.255+185_255+186insAC ENSP00000305426.4:n.255+185_255+186insAC
ENST00000534099.5:c.108+185_108+186insAC ENSP00000434400.1:n.108+185_108+186insAC
NM_003320.4:c.255+185_255+186insAC NP_003311.2:n.255+185_255+186insAC
NM_177972.2:c.90+185_90+186insAC NP_813977.1:n.90+185_90+186insAC
XM_005253109.2:c.216+185_216+186insAC XP_005253166.1:n.216+185_216+186insAC
XM_011520344.1:c.126+185_126+186insAC XP_011518646.1:n.126+185_126+186insAC
XM_005253109.3:c.216+185_216+186insAC XP_005253166.1:n.216+185_216+186insAC
XM_011520344.2:c.126+185_126+186insAC XP_011518646.1:n.126+185_126+186insAC
NM_177972.3:c.90+185_90+186insAC MANE Select NP_813977.1:n.90+185_90+186insAC
NM_003320.5:c.255+185_255+186insAC NP_003311.2:n.255+185_255+186insAC
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