Canonical Allele Identifier: CA2612334145

Linked Data

gnomAD v4: 11-8101827-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101827T>C , CM000673.2:g.8101827T>C GRCh38
NC_000011.9:g.8123374T>C , CM000673.1:g.8123374T>C GRCh37
NC_000011.8:g.8079950T>C NCBI36
NG_029912.1:g.68195T>C
NG_030416.2:g.72217A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*208T>C (TUB) MANE Select ENSP00000299506.3:n.*208T>C
ENST00000299506.2:c.*208T>C (TUB) ENSP00000299506.2:n.*208T>C
ENST00000305253.8:c.*208T>C (TUB) ENSP00000305426.4:n.*208T>C
NM_003320.4:c.*208T>C (TUB) NP_003311.2:n.*208T>C
NM_177972.2:c.*208T>C (TUB) NP_813977.1:n.*208T>C
XM_005253109.2:c.*208T>C (TUB) XP_005253166.1:n.*208T>C
XM_011520344.1:c.*208T>C (TUB) XP_011518646.1:n.*208T>C
XR_428851.2:n.1484-7668A>G (RIC3)
XR_930896.1:n.1546+5508A>G (RIC3)
XR_930900.1:n.1547-4105A>G (RIC3)
NR_144485.1:n.1519+5508A>G (RIC3)
XM_005253109.3:c.*208T>C (TUB) XP_005253166.1:n.*208T>C
XM_011520344.2:c.*208T>C (TUB) XP_011518646.1:n.*208T>C
XR_001747957.2:n.1335-7668A>G (RIC3)
XR_428851.4:n.1422-7668A>G (RIC3)
XR_930896.3:n.1484+5508A>G (RIC3)
XR_930900.3:n.1485-4105A>G (RIC3)
NM_177972.3:c.*208T>C (TUB) MANE Select NP_813977.1:n.*208T>C
NR_144485.2:n.1450+5508A>G (RIC3)
NM_003320.5:c.*208T>C (TUB) NP_003311.2:n.*208T>C