Canonical Allele Identifier: CA2612334016

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101775_8101776insGG , CM000673.2:g.8101775_8101776insGG GRCh38
NC_000011.9:g.8123322_8123323insGG , CM000673.1:g.8123322_8123323insGG GRCh37
NC_000011.8:g.8079898_8079899insGG NCBI36
NG_029912.1:g.68143_68144insGG
NG_030416.2:g.72268_72269insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*156_*157insGG (TUB) MANE Select ENSP00000299506.3:n.*156_*157insGG
ENST00000299506.2:c.*156_*157insGG (TUB) ENSP00000299506.2:n.*156_*157insGG
ENST00000305253.8:c.*156_*157insGG (TUB) ENSP00000305426.4:n.*156_*157insGG
ENST00000534099.5:c.*156_*157insGG (TUB) ENSP00000434400.1:n.*156_*157insGG
NM_003320.4:c.*156_*157insGG (TUB) NP_003311.2:n.*156_*157insGG
NM_177972.2:c.*156_*157insGG (TUB) NP_813977.1:n.*156_*157insGG
XM_005253109.2:c.*156_*157insGG (TUB) XP_005253166.1:n.*156_*157insGG
XM_011520344.1:c.*156_*157insGG (TUB) XP_011518646.1:n.*156_*157insGG
XR_428851.2:n.1484-7617_1484-7616insCC (RIC3)
XR_930896.1:n.1546+5559_1546+5560insCC (RIC3)
XR_930900.1:n.1547-4054_1547-4053insCC (RIC3)
NR_144485.1:n.1519+5559_1519+5560insCC (RIC3)
XM_005253109.3:c.*156_*157insGG (TUB) XP_005253166.1:n.*156_*157insGG
XM_011520344.2:c.*156_*157insGG (TUB) XP_011518646.1:n.*156_*157insGG
XR_001747957.2:n.1335-7617_1335-7616insCC (RIC3)
XR_428851.4:n.1422-7617_1422-7616insCC (RIC3)
XR_930896.3:n.1484+5559_1484+5560insCC (RIC3)
XR_930900.3:n.1485-4054_1485-4053insCC (RIC3)
NM_177972.3:c.*156_*157insGG (TUB) MANE Select NP_813977.1:n.*156_*157insGG
NR_144485.2:n.1450+5559_1450+5560insCC (RIC3)
NM_003320.5:c.*156_*157insGG (TUB) NP_003311.2:n.*156_*157insGG