Canonical Allele Identifier: CA2790353725

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101825_8101826insTT , CM000673.2:g.8101825_8101826insTT GRCh38
NC_000011.9:g.8123372_8123373insTT , CM000673.1:g.8123372_8123373insTT GRCh37
NC_000011.8:g.8079948_8079949insTT NCBI36
NG_029912.1:g.68193_68194insTT
NG_030416.2:g.72218_72219insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*206_*207insTT (TUB) MANE Select ENSP00000299506.3:n.*206_*207insTT
ENST00000299506.2:c.*206_*207insTT (TUB) ENSP00000299506.2:n.*206_*207insTT
ENST00000305253.8:c.*206_*207insTT (TUB) ENSP00000305426.4:n.*206_*207insTT
NM_003320.4:c.*206_*207insTT (TUB) NP_003311.2:n.*206_*207insTT
NM_177972.2:c.*206_*207insTT (TUB) NP_813977.1:n.*206_*207insTT
XM_005253109.2:c.*206_*207insTT (TUB) XP_005253166.1:n.*206_*207insTT
XM_011520344.1:c.*206_*207insTT (TUB) XP_011518646.1:n.*206_*207insTT
XR_428851.2:n.1484-7667_1484-7666insAA (RIC3)
XR_930896.1:n.1546+5509_1546+5510insAA (RIC3)
XR_930900.1:n.1547-4104_1547-4103insAA (RIC3)
NR_144485.1:n.1519+5509_1519+5510insAA (RIC3)
XM_005253109.3:c.*206_*207insTT (TUB) XP_005253166.1:n.*206_*207insTT
XM_011520344.2:c.*206_*207insTT (TUB) XP_011518646.1:n.*206_*207insTT
XR_001747957.2:n.1335-7667_1335-7666insAA (RIC3)
XR_428851.4:n.1422-7667_1422-7666insAA (RIC3)
XR_930896.3:n.1484+5509_1484+5510insAA (RIC3)
XR_930900.3:n.1485-4104_1485-4103insAA (RIC3)
NM_177972.3:c.*206_*207insTT (TUB) MANE Select NP_813977.1:n.*206_*207insTT
NR_144485.2:n.1450+5509_1450+5510insAA (RIC3)
NM_003320.5:c.*206_*207insTT (TUB) NP_003311.2:n.*206_*207insTT