Canonical Allele Identifier: CA934892992

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101837_8101838insTT , CM000673.2:g.8101837_8101838insTT GRCh38
NC_000011.9:g.8123384_8123385insTT , CM000673.1:g.8123384_8123385insTT GRCh37
NC_000011.8:g.8079960_8079961insTT NCBI36
NG_029912.1:g.68205_68206insTT
NG_030416.2:g.72207_72208insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*218_*219insTT (TUB) MANE Select ENSP00000299506.3:n.*218_*219insTT
ENST00000299506.2:c.*218_*219insTT (TUB) ENSP00000299506.2:n.*218_*219insTT
ENST00000305253.8:c.*218_*219insTT (TUB) ENSP00000305426.4:n.*218_*219insTT
NM_003320.4:c.*218_*219insTT (TUB) NP_003311.2:n.*218_*219insTT
NM_177972.2:c.*218_*219insTT (TUB) NP_813977.1:n.*218_*219insTT
XM_005253109.2:c.*218_*219insTT (TUB) XP_005253166.1:n.*218_*219insTT
XM_011520344.1:c.*218_*219insTT (TUB) XP_011518646.1:n.*218_*219insTT
XR_428851.2:n.1484-7678_1484-7677insAA (RIC3)
XR_930896.1:n.1546+5498_1546+5499insAA (RIC3)
XR_930900.1:n.1547-4115_1547-4114insAA (RIC3)
NR_144485.1:n.1519+5498_1519+5499insAA (RIC3)
XM_005253109.3:c.*218_*219insTT (TUB) XP_005253166.1:n.*218_*219insTT
XM_011520344.2:c.*218_*219insTT (TUB) XP_011518646.1:n.*218_*219insTT
XR_001747957.2:n.1335-7678_1335-7677insAA (RIC3)
XR_428851.4:n.1422-7678_1422-7677insAA (RIC3)
XR_930896.3:n.1484+5498_1484+5499insAA (RIC3)
XR_930900.3:n.1485-4115_1485-4114insAA (RIC3)
NM_177972.3:c.*218_*219insTT (TUB) MANE Select NP_813977.1:n.*218_*219insTT
NR_144485.2:n.1450+5498_1450+5499insAA (RIC3)
NM_003320.5:c.*218_*219insTT (TUB) NP_003311.2:n.*218_*219insTT