Canonical Allele Identifier: CA2612334861

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101973_8101974insT , CM000673.2:g.8101973_8101974insT GRCh38
NC_000011.9:g.8123520_8123521insT , CM000673.1:g.8123520_8123521insT GRCh37
NC_000011.8:g.8080096_8080097insT NCBI36
NG_029912.1:g.68341_68342insT
NG_030416.2:g.72070_72071insA

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*354_*355insT (TUB) MANE Select ENSP00000299506.3:n.*354_*355insT
ENST00000305253.8:c.*354_*355insT (TUB) ENSP00000305426.4:n.*354_*355insT
NM_003320.4:c.*354_*355insT (TUB) NP_003311.2:n.*354_*355insT
NM_177972.2:c.*354_*355insT (TUB) NP_813977.1:n.*354_*355insT
XM_005253109.2:c.*354_*355insT (TUB) XP_005253166.1:n.*354_*355insT
XM_011520344.1:c.*354_*355insT (TUB) XP_011518646.1:n.*354_*355insT
XR_428851.2:n.1484-7815_1484-7814insA (RIC3)
XR_930896.1:n.1546+5361_1546+5362insA (RIC3)
XR_930900.1:n.1547-4252_1547-4251insA (RIC3)
NR_144485.1:n.1519+5361_1519+5362insA (RIC3)
XM_005253109.3:c.*354_*355insT (TUB) XP_005253166.1:n.*354_*355insT
XM_011520344.2:c.*354_*355insT (TUB) XP_011518646.1:n.*354_*355insT
XR_001747957.2:n.1335-7815_1335-7814insA (RIC3)
XR_428851.4:n.1422-7815_1422-7814insA (RIC3)
XR_930896.3:n.1484+5361_1484+5362insA (RIC3)
XR_930900.3:n.1485-4252_1485-4251insA (RIC3)
NM_177972.3:c.*354_*355insT (TUB) MANE Select NP_813977.1:n.*354_*355insT
NR_144485.2:n.1450+5361_1450+5362insA (RIC3)
NM_003320.5:c.*354_*355insT (TUB) NP_003311.2:n.*354_*355insT