Canonical Allele Identifier: CA2790351841
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089841_8089842insACA , CM000673.2:g.8089841_8089842insACA GRCh38
NC_000011.9:g.8111388_8111389insACA , CM000673.1:g.8111388_8111389insACA GRCh37
NC_000011.8:g.8067964_8067965insACA NCBI36
NG_029912.1:g.56209_56210insACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.90+180_90+181insACA MANE Select ENSP00000299506.3:n.90+180_90+181insACA
ENST00000299506.2:c.90+180_90+181insACA ENSP00000299506.2:n.90+180_90+181insACA
ENST00000305253.8:c.255+180_255+181insACA ENSP00000305426.4:n.255+180_255+181insACA
ENST00000534099.5:c.108+180_108+181insACA ENSP00000434400.1:n.108+180_108+181insACA
NM_003320.4:c.255+180_255+181insACA NP_003311.2:n.255+180_255+181insACA
NM_177972.2:c.90+180_90+181insACA NP_813977.1:n.90+180_90+181insACA
XM_005253109.2:c.216+180_216+181insACA XP_005253166.1:n.216+180_216+181insACA
XM_011520344.1:c.126+180_126+181insACA XP_011518646.1:n.126+180_126+181insACA
XM_005253109.3:c.216+180_216+181insACA XP_005253166.1:n.216+180_216+181insACA
XM_011520344.2:c.126+180_126+181insACA XP_011518646.1:n.126+180_126+181insACA
NM_177972.3:c.90+180_90+181insACA MANE Select NP_813977.1:n.90+180_90+181insACA
NM_003320.5:c.255+180_255+181insACA NP_003311.2:n.255+180_255+181insACA