Canonical Allele Identifier: CA2612334036

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101786_8101787insA , CM000673.2:g.8101786_8101787insA GRCh38
NC_000011.9:g.8123333_8123334insA , CM000673.1:g.8123333_8123334insA GRCh37
NC_000011.8:g.8079909_8079910insA NCBI36
NG_029912.1:g.68154_68155insA
NG_030416.2:g.72257_72258insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*167_*168insA (TUB) MANE Select ENSP00000299506.3:n.*167_*168insA
ENST00000299506.2:c.*167_*168insA (TUB) ENSP00000299506.2:n.*167_*168insA
ENST00000305253.8:c.*167_*168insA (TUB) ENSP00000305426.4:n.*167_*168insA
NM_003320.4:c.*167_*168insA (TUB) NP_003311.2:n.*167_*168insA
NM_177972.2:c.*167_*168insA (TUB) NP_813977.1:n.*167_*168insA
XM_005253109.2:c.*167_*168insA (TUB) XP_005253166.1:n.*167_*168insA
XM_011520344.1:c.*167_*168insA (TUB) XP_011518646.1:n.*167_*168insA
XR_428851.2:n.1484-7628_1484-7627insT (RIC3)
XR_930896.1:n.1546+5548_1546+5549insT (RIC3)
XR_930900.1:n.1547-4065_1547-4064insT (RIC3)
NR_144485.1:n.1519+5548_1519+5549insT (RIC3)
XM_005253109.3:c.*167_*168insA (TUB) XP_005253166.1:n.*167_*168insA
XM_011520344.2:c.*167_*168insA (TUB) XP_011518646.1:n.*167_*168insA
XR_001747957.2:n.1335-7628_1335-7627insT (RIC3)
XR_428851.4:n.1422-7628_1422-7627insT (RIC3)
XR_930896.3:n.1484+5548_1484+5549insT (RIC3)
XR_930900.3:n.1485-4065_1485-4064insT (RIC3)
NM_177972.3:c.*167_*168insA (TUB) MANE Select NP_813977.1:n.*167_*168insA
NR_144485.2:n.1450+5548_1450+5549insT (RIC3)
NM_003320.5:c.*167_*168insA (TUB) NP_003311.2:n.*167_*168insA