Canonical Allele Identifier: CA1950968187

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101758_8101759delinsGC , CM000673.2:g.8101758_8101759delinsGC GRCh38
NC_000011.9:g.8123305_8123306delinsGC , CM000673.1:g.8123305_8123306delinsGC GRCh37
NC_000011.8:g.8079881_8079882delinsGC NCBI36
NG_029912.1:g.68126_68127delinsGC
NG_030416.2:g.72285_72286delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*139_*140delinsGC (TUB) MANE Select ENSP00000299506.3:n.*139_*140delinsGC
ENST00000299506.2:c.*139_*140delinsGC (TUB) ENSP00000299506.2:n.*139_*140delinsGC
ENST00000305253.8:c.*139_*140delinsGC (TUB) ENSP00000305426.4:n.*139_*140delinsGC
ENST00000534099.5:c.*139_*140delinsGC (TUB) ENSP00000434400.1:n.*139_*140delinsGC
NM_003320.4:c.*139_*140delinsGC (TUB) NP_003311.2:n.*139_*140delinsGC
NM_177972.2:c.*139_*140delinsGC (TUB) NP_813977.1:n.*139_*140delinsGC
XM_005253109.2:c.*139_*140delinsGC (TUB) XP_005253166.1:n.*139_*140delinsGC
XM_011520344.1:c.*139_*140delinsGC (TUB) XP_011518646.1:n.*139_*140delinsGC
XR_428851.2:n.1484-7600_1484-7599delinsGC (RIC3)
XR_930896.1:n.1546+5576_1546+5577delinsGC (RIC3)
XR_930900.1:n.1547-4037_1547-4036delinsGC (RIC3)
NR_144485.1:n.1519+5576_1519+5577delinsGC (RIC3)
XM_005253109.3:c.*139_*140delinsGC (TUB) XP_005253166.1:n.*139_*140delinsGC
XM_011520344.2:c.*139_*140delinsGC (TUB) XP_011518646.1:n.*139_*140delinsGC
XR_001747957.2:n.1335-7600_1335-7599delinsGC (RIC3)
XR_428851.4:n.1422-7600_1422-7599delinsGC (RIC3)
XR_930896.3:n.1484+5576_1484+5577delinsGC (RIC3)
XR_930900.3:n.1485-4037_1485-4036delinsGC (RIC3)
NM_177972.3:c.*139_*140delinsGC (TUB) MANE Select NP_813977.1:n.*139_*140delinsGC
NR_144485.2:n.1450+5576_1450+5577delinsGC (RIC3)
NM_003320.5:c.*139_*140delinsGC (TUB) NP_003311.2:n.*139_*140delinsGC