Canonical Allele Identifier: CA2612334047

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101790_8101791insG , CM000673.2:g.8101790_8101791insG GRCh38
NC_000011.9:g.8123337_8123338insG , CM000673.1:g.8123337_8123338insG GRCh37
NC_000011.8:g.8079913_8079914insG NCBI36
NG_029912.1:g.68158_68159insG
NG_030416.2:g.72253_72254insC

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*171_*172insG (TUB) MANE Select ENSP00000299506.3:n.*171_*172insG
ENST00000299506.2:c.*171_*172insG (TUB) ENSP00000299506.2:n.*171_*172insG
ENST00000305253.8:c.*171_*172insG (TUB) ENSP00000305426.4:n.*171_*172insG
NM_003320.4:c.*171_*172insG (TUB) NP_003311.2:n.*171_*172insG
NM_177972.2:c.*171_*172insG (TUB) NP_813977.1:n.*171_*172insG
XM_005253109.2:c.*171_*172insG (TUB) XP_005253166.1:n.*171_*172insG
XM_011520344.1:c.*171_*172insG (TUB) XP_011518646.1:n.*171_*172insG
XR_428851.2:n.1484-7632_1484-7631insC (RIC3)
XR_930896.1:n.1546+5544_1546+5545insC (RIC3)
XR_930900.1:n.1547-4069_1547-4068insC (RIC3)
NR_144485.1:n.1519+5544_1519+5545insC (RIC3)
XM_005253109.3:c.*171_*172insG (TUB) XP_005253166.1:n.*171_*172insG
XM_011520344.2:c.*171_*172insG (TUB) XP_011518646.1:n.*171_*172insG
XR_001747957.2:n.1335-7632_1335-7631insC (RIC3)
XR_428851.4:n.1422-7632_1422-7631insC (RIC3)
XR_930896.3:n.1484+5544_1484+5545insC (RIC3)
XR_930900.3:n.1485-4069_1485-4068insC (RIC3)
NM_177972.3:c.*171_*172insG (TUB) MANE Select NP_813977.1:n.*171_*172insG
NR_144485.2:n.1450+5544_1450+5545insC (RIC3)
NM_003320.5:c.*171_*172insG (TUB) NP_003311.2:n.*171_*172insG