Canonical Allele Identifier: CA2612334363

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101850_8101851insAAT , CM000673.2:g.8101850_8101851insAAT GRCh38
NC_000011.9:g.8123397_8123398insAAT , CM000673.1:g.8123397_8123398insAAT GRCh37
NC_000011.8:g.8079973_8079974insAAT NCBI36
NG_029912.1:g.68218_68219insAAT
NG_030416.2:g.72194_72195insTTA

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*231_*232insAAT (TUB) MANE Select ENSP00000299506.3:n.*231_*232insAAT
ENST00000299506.2:c.*231_*232insAAT (TUB) ENSP00000299506.2:n.*231_*232insAAT
ENST00000305253.8:c.*231_*232insAAT (TUB) ENSP00000305426.4:n.*231_*232insAAT
NM_003320.4:c.*231_*232insAAT (TUB) NP_003311.2:n.*231_*232insAAT
NM_177972.2:c.*231_*232insAAT (TUB) NP_813977.1:n.*231_*232insAAT
XM_005253109.2:c.*231_*232insAAT (TUB) XP_005253166.1:n.*231_*232insAAT
XM_011520344.1:c.*231_*232insAAT (TUB) XP_011518646.1:n.*231_*232insAAT
XR_428851.2:n.1484-7691_1484-7690insTTA (RIC3)
XR_930896.1:n.1546+5485_1546+5486insTTA (RIC3)
XR_930900.1:n.1547-4128_1547-4127insTTA (RIC3)
NR_144485.1:n.1519+5485_1519+5486insTTA (RIC3)
XM_005253109.3:c.*231_*232insAAT (TUB) XP_005253166.1:n.*231_*232insAAT
XM_011520344.2:c.*231_*232insAAT (TUB) XP_011518646.1:n.*231_*232insAAT
XR_001747957.2:n.1335-7691_1335-7690insTTA (RIC3)
XR_428851.4:n.1422-7691_1422-7690insTTA (RIC3)
XR_930896.3:n.1484+5485_1484+5486insTTA (RIC3)
XR_930900.3:n.1485-4128_1485-4127insTTA (RIC3)
NM_177972.3:c.*231_*232insAAT (TUB) MANE Select NP_813977.1:n.*231_*232insAAT
NR_144485.2:n.1450+5485_1450+5486insTTA (RIC3)
NM_003320.5:c.*231_*232insAAT (TUB) NP_003311.2:n.*231_*232insAAT