Canonical Allele Identifier: CA2612334141

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101827_8101830del , CM000673.2:g.8101827_8101830del GRCh38
NC_000011.9:g.8123374_8123377del , CM000673.1:g.8123374_8123377del GRCh37
NC_000011.8:g.8079950_8079953del NCBI36
NG_029912.1:g.68195_68198del
NG_030416.2:g.72215_72218del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*208_*211del (TUB) MANE Select ENSP00000299506.3:n.*208_*211del
ENST00000299506.2:c.*208_*211del (TUB) ENSP00000299506.2:n.*208_*211del
ENST00000305253.8:c.*208_*211del (TUB) ENSP00000305426.4:n.*208_*211del
NM_003320.4:c.*208_*211del (TUB) NP_003311.2:n.*208_*211del
NM_177972.2:c.*208_*211del (TUB) NP_813977.1:n.*208_*211del
XM_005253109.2:c.*208_*211del (TUB) XP_005253166.1:n.*208_*211del
XM_011520344.1:c.*208_*211del (TUB) XP_011518646.1:n.*208_*211del
XR_428851.2:n.1484-7670_1484-7667del (RIC3)
XR_930896.1:n.1546+5506_1546+5509del (RIC3)
XR_930900.1:n.1547-4107_1547-4104del (RIC3)
NR_144485.1:n.1519+5506_1519+5509del (RIC3)
XM_005253109.3:c.*208_*211del (TUB) XP_005253166.1:n.*208_*211del
XM_011520344.2:c.*208_*211del (TUB) XP_011518646.1:n.*208_*211del
XR_001747957.2:n.1335-7670_1335-7667del (RIC3)
XR_428851.4:n.1422-7670_1422-7667del (RIC3)
XR_930896.3:n.1484+5506_1484+5509del (RIC3)
XR_930900.3:n.1485-4107_1485-4104del (RIC3)
NM_177972.3:c.*208_*211del (TUB) MANE Select NP_813977.1:n.*208_*211del
NR_144485.2:n.1450+5506_1450+5509del (RIC3)
NM_003320.5:c.*208_*211del (TUB) NP_003311.2:n.*208_*211del