Canonical Allele Identifier: CA2612334382

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101850_8101851insAAAGA , CM000673.2:g.8101850_8101851insAAAGA GRCh38
NC_000011.9:g.8123397_8123398insAAAGA , CM000673.1:g.8123397_8123398insAAAGA GRCh37
NC_000011.8:g.8079973_8079974insAAAGA NCBI36
NG_029912.1:g.68218_68219insAAAGA
NG_030416.2:g.72193_72194insTCTTT

Transcript Alleles

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