Canonical Allele Identifier: CA1950968080

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101675_8101679delinsCCTGT , CM000673.2:g.8101675_8101679delinsCCTGT GRCh38
NC_000011.9:g.8123222_8123226delinsCCTGT , CM000673.1:g.8123222_8123226delinsCCTGT GRCh37
NC_000011.8:g.8079798_8079802delinsCCTGT NCBI36
NG_029912.1:g.68043_68047delinsCCTGT
NG_030416.2:g.72365_72369delinsACAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*56_*60delinsCCTGT (TUB) MANE Select ENSP00000299506.3:n.*56_*60delinsCCTGT
ENST00000299506.2:c.*56_*60delinsCCTGT (TUB) ENSP00000299506.2:n.*56_*60delinsCCTGT
ENST00000305253.8:c.*56_*60delinsCCTGT (TUB) ENSP00000305426.4:n.*56_*60delinsCCTGT
ENST00000534099.5:c.*56_*60delinsCCTGT (TUB) ENSP00000434400.1:n.*56_*60delinsCCTGT
NM_003320.4:c.*56_*60delinsCCTGT (TUB) NP_003311.2:n.*56_*60delinsCCTGT
NM_177972.2:c.*56_*60delinsCCTGT (TUB) NP_813977.1:n.*56_*60delinsCCTGT
XM_005253109.2:c.*56_*60delinsCCTGT (TUB) XP_005253166.1:n.*56_*60delinsCCTGT
XM_011520344.1:c.*56_*60delinsCCTGT (TUB) XP_011518646.1:n.*56_*60delinsCCTGT
XR_428851.2:n.1484-7520_1484-7516delinsACAGG (RIC3)
XR_930896.1:n.1546+5656_1546+5660delinsACAGG (RIC3)
XR_930900.1:n.1547-3957_1547-3953delinsACAGG (RIC3)
NR_144485.1:n.1519+5656_1519+5660delinsACAGG (RIC3)
XM_005253109.3:c.*56_*60delinsCCTGT (TUB) XP_005253166.1:n.*56_*60delinsCCTGT
XM_011520344.2:c.*56_*60delinsCCTGT (TUB) XP_011518646.1:n.*56_*60delinsCCTGT
XR_001747957.2:n.1335-7520_1335-7516delinsACAGG (RIC3)
XR_428851.4:n.1422-7520_1422-7516delinsACAGG (RIC3)
XR_930896.3:n.1484+5656_1484+5660delinsACAGG (RIC3)
XR_930900.3:n.1485-3957_1485-3953delinsACAGG (RIC3)
NM_177972.3:c.*56_*60delinsCCTGT (TUB) MANE Select NP_813977.1:n.*56_*60delinsCCTGT
NR_144485.2:n.1450+5656_1450+5660delinsACAGG (RIC3)
NM_003320.5:c.*56_*60delinsCCTGT (TUB) NP_003311.2:n.*56_*60delinsCCTGT