Canonical Allele Identifier: CA2790353747

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101850_8101851insAC , CM000673.2:g.8101850_8101851insAC GRCh38
NC_000011.9:g.8123397_8123398insAC , CM000673.1:g.8123397_8123398insAC GRCh37
NC_000011.8:g.8079973_8079974insAC NCBI36
NG_029912.1:g.68218_68219insAC
NG_030416.2:g.72193_72194insGT

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*231_*232insAC (TUB) MANE Select ENSP00000299506.3:n.*231_*232insAC
ENST00000299506.2:c.*231_*232insAC (TUB) ENSP00000299506.2:n.*231_*232insAC
ENST00000305253.8:c.*231_*232insAC (TUB) ENSP00000305426.4:n.*231_*232insAC
NM_003320.4:c.*231_*232insAC (TUB) NP_003311.2:n.*231_*232insAC
NM_177972.2:c.*231_*232insAC (TUB) NP_813977.1:n.*231_*232insAC
XM_005253109.2:c.*231_*232insAC (TUB) XP_005253166.1:n.*231_*232insAC
XM_011520344.1:c.*231_*232insAC (TUB) XP_011518646.1:n.*231_*232insAC
XR_428851.2:n.1484-7692_1484-7691insGT (RIC3)
XR_930896.1:n.1546+5484_1546+5485insGT (RIC3)
XR_930900.1:n.1547-4129_1547-4128insGT (RIC3)
NR_144485.1:n.1519+5484_1519+5485insGT (RIC3)
XM_005253109.3:c.*231_*232insAC (TUB) XP_005253166.1:n.*231_*232insAC
XM_011520344.2:c.*231_*232insAC (TUB) XP_011518646.1:n.*231_*232insAC
XR_001747957.2:n.1335-7692_1335-7691insGT (RIC3)
XR_428851.4:n.1422-7692_1422-7691insGT (RIC3)
XR_930896.3:n.1484+5484_1484+5485insGT (RIC3)
XR_930900.3:n.1485-4129_1485-4128insGT (RIC3)
NM_177972.3:c.*231_*232insAC (TUB) MANE Select NP_813977.1:n.*231_*232insAC
NR_144485.2:n.1450+5484_1450+5485insGT (RIC3)
NM_003320.5:c.*231_*232insAC (TUB) NP_003311.2:n.*231_*232insAC