Canonical Allele Identifier: CA2612334142

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101829_8101830del , CM000673.2:g.8101829_8101830del GRCh38
NC_000011.9:g.8123376_8123377del , CM000673.1:g.8123376_8123377del GRCh37
NC_000011.8:g.8079952_8079953del NCBI36
NG_029912.1:g.68197_68198del
NG_030416.2:g.72217_72218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*210_*211del (TUB) MANE Select ENSP00000299506.3:n.*210_*211del
ENST00000299506.2:c.*210_*211del (TUB) ENSP00000299506.2:n.*210_*211del
ENST00000305253.8:c.*210_*211del (TUB) ENSP00000305426.4:n.*210_*211del
NM_003320.4:c.*210_*211del (TUB) NP_003311.2:n.*210_*211del
NM_177972.2:c.*210_*211del (TUB) NP_813977.1:n.*210_*211del
XM_005253109.2:c.*210_*211del (TUB) XP_005253166.1:n.*210_*211del
XM_011520344.1:c.*210_*211del (TUB) XP_011518646.1:n.*210_*211del
XR_428851.2:n.1484-7668_1484-7667del (RIC3)
XR_930896.1:n.1546+5508_1546+5509del (RIC3)
XR_930900.1:n.1547-4105_1547-4104del (RIC3)
NR_144485.1:n.1519+5508_1519+5509del (RIC3)
XM_005253109.3:c.*210_*211del (TUB) XP_005253166.1:n.*210_*211del
XM_011520344.2:c.*210_*211del (TUB) XP_011518646.1:n.*210_*211del
XR_001747957.2:n.1335-7668_1335-7667del (RIC3)
XR_428851.4:n.1422-7668_1422-7667del (RIC3)
XR_930896.3:n.1484+5508_1484+5509del (RIC3)
XR_930900.3:n.1485-4105_1485-4104del (RIC3)
NM_177972.3:c.*210_*211del (TUB) MANE Select NP_813977.1:n.*210_*211del
NR_144485.2:n.1450+5508_1450+5509del (RIC3)
NM_003320.5:c.*210_*211del (TUB) NP_003311.2:n.*210_*211del