Canonical Allele Identifier: CA2790351848
Gene: TUB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089842_8089843insA , CM000673.2:g.8089842_8089843insA GRCh38
NC_000011.9:g.8111389_8111390insA , CM000673.1:g.8111389_8111390insA GRCh37
NC_000011.8:g.8067965_8067966insA NCBI36
NG_029912.1:g.56210_56211insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.90+181_90+182insA MANE Select ENSP00000299506.3:n.90+181_90+182insA
ENST00000299506.2:c.90+181_90+182insA ENSP00000299506.2:n.90+181_90+182insA
ENST00000305253.8:c.255+181_255+182insA ENSP00000305426.4:n.255+181_255+182insA
ENST00000534099.5:c.108+181_108+182insA ENSP00000434400.1:n.108+181_108+182insA
NM_003320.4:c.255+181_255+182insA NP_003311.2:n.255+181_255+182insA
NM_177972.2:c.90+181_90+182insA NP_813977.1:n.90+181_90+182insA
XM_005253109.2:c.216+181_216+182insA XP_005253166.1:n.216+181_216+182insA
XM_011520344.1:c.126+181_126+182insA XP_011518646.1:n.126+181_126+182insA
XM_005253109.3:c.216+181_216+182insA XP_005253166.1:n.216+181_216+182insA
XM_011520344.2:c.126+181_126+182insA XP_011518646.1:n.126+181_126+182insA
NM_177972.3:c.90+181_90+182insA MANE Select NP_813977.1:n.90+181_90+182insA
NM_003320.5:c.255+181_255+182insA NP_003311.2:n.255+181_255+182insA
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