Canonical Allele Identifier: CA1950968480

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8102046_8102047delinsTA , CM000673.2:g.8102046_8102047delinsTA GRCh38
NC_000011.9:g.8123593_8123594delinsTA , CM000673.1:g.8123593_8123594delinsTA GRCh37
NC_000011.8:g.8080169_8080170delinsTA NCBI36
NG_029912.1:g.68414_68415delinsTA
NG_030416.2:g.71997_71998delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*427_*428delinsTA (TUB) MANE Select ENSP00000299506.3:n.*427_*428delinsTA
ENST00000305253.8:c.*427_*428delinsTA (TUB) ENSP00000305426.4:n.*427_*428delinsTA
NM_003320.4:c.*427_*428delinsTA (TUB) NP_003311.2:n.*427_*428delinsTA
NM_177972.2:c.*427_*428delinsTA (TUB) NP_813977.1:n.*427_*428delinsTA
XM_005253109.2:c.*427_*428delinsTA (TUB) XP_005253166.1:n.*427_*428delinsTA
XM_011520344.1:c.*427_*428delinsTA (TUB) XP_011518646.1:n.*427_*428delinsTA
XR_428851.2:n.1484-7888_1484-7887delinsTA (RIC3)
XR_930896.1:n.1546+5288_1546+5289delinsTA (RIC3)
XR_930900.1:n.1547-4325_1547-4324delinsTA (RIC3)
NR_144485.1:n.1519+5288_1519+5289delinsTA (RIC3)
XM_005253109.3:c.*427_*428delinsTA (TUB) XP_005253166.1:n.*427_*428delinsTA
XM_011520344.2:c.*427_*428delinsTA (TUB) XP_011518646.1:n.*427_*428delinsTA
XR_001747957.2:n.1335-7888_1335-7887delinsTA (RIC3)
XR_428851.4:n.1422-7888_1422-7887delinsTA (RIC3)
XR_930896.3:n.1484+5288_1484+5289delinsTA (RIC3)
XR_930900.3:n.1485-4325_1485-4324delinsTA (RIC3)
NM_177972.3:c.*427_*428delinsTA (TUB) MANE Select NP_813977.1:n.*427_*428delinsTA
NR_144485.2:n.1450+5288_1450+5289delinsTA (RIC3)
NM_003320.5:c.*427_*428delinsTA (TUB) NP_003311.2:n.*427_*428delinsTA