Canonical Allele Identifier: CA2612334565

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101860_8101861insA , CM000673.2:g.8101860_8101861insA GRCh38
NC_000011.9:g.8123407_8123408insA , CM000673.1:g.8123407_8123408insA GRCh37
NC_000011.8:g.8079983_8079984insA NCBI36
NG_029912.1:g.68228_68229insA
NG_030416.2:g.72183_72184insT

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*241_*242insA (TUB) MANE Select ENSP00000299506.3:n.*241_*242insA
ENST00000299506.2:c.*241_*242insA (TUB) ENSP00000299506.2:n.*241_*242insA
ENST00000305253.8:c.*241_*242insA (TUB) ENSP00000305426.4:n.*241_*242insA
NM_003320.4:c.*241_*242insA (TUB) NP_003311.2:n.*241_*242insA
NM_177972.2:c.*241_*242insA (TUB) NP_813977.1:n.*241_*242insA
XM_005253109.2:c.*241_*242insA (TUB) XP_005253166.1:n.*241_*242insA
XM_011520344.1:c.*241_*242insA (TUB) XP_011518646.1:n.*241_*242insA
XR_428851.2:n.1484-7702_1484-7701insT (RIC3)
XR_930896.1:n.1546+5474_1546+5475insT (RIC3)
XR_930900.1:n.1547-4139_1547-4138insT (RIC3)
NR_144485.1:n.1519+5474_1519+5475insT (RIC3)
XM_005253109.3:c.*241_*242insA (TUB) XP_005253166.1:n.*241_*242insA
XM_011520344.2:c.*241_*242insA (TUB) XP_011518646.1:n.*241_*242insA
XR_001747957.2:n.1335-7702_1335-7701insT (RIC3)
XR_428851.4:n.1422-7702_1422-7701insT (RIC3)
XR_930896.3:n.1484+5474_1484+5475insT (RIC3)
XR_930900.3:n.1485-4139_1485-4138insT (RIC3)
NM_177972.3:c.*241_*242insA (TUB) MANE Select NP_813977.1:n.*241_*242insA
NR_144485.2:n.1450+5474_1450+5475insT (RIC3)
NM_003320.5:c.*241_*242insA (TUB) NP_003311.2:n.*241_*242insA