Canonical Allele Identifier: CA2612334149

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101828_8101831del , CM000673.2:g.8101828_8101831del GRCh38
NC_000011.9:g.8123375_8123378del , CM000673.1:g.8123375_8123378del GRCh37
NC_000011.8:g.8079951_8079954del NCBI36
NG_029912.1:g.68196_68199del
NG_030416.2:g.72213_72216del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*209_*212del (TUB) MANE Select ENSP00000299506.3:n.*209_*212del
ENST00000299506.2:c.*209_*212del (TUB) ENSP00000299506.2:n.*209_*212del
ENST00000305253.8:c.*209_*212del (TUB) ENSP00000305426.4:n.*209_*212del
NM_003320.4:c.*209_*212del (TUB) NP_003311.2:n.*209_*212del
NM_177972.2:c.*209_*212del (TUB) NP_813977.1:n.*209_*212del
XM_005253109.2:c.*209_*212del (TUB) XP_005253166.1:n.*209_*212del
XM_011520344.1:c.*209_*212del (TUB) XP_011518646.1:n.*209_*212del
XR_428851.2:n.1484-7672_1484-7669del (RIC3)
XR_930896.1:n.1546+5504_1546+5507del (RIC3)
XR_930900.1:n.1547-4109_1547-4106del (RIC3)
NR_144485.1:n.1519+5504_1519+5507del (RIC3)
XM_005253109.3:c.*209_*212del (TUB) XP_005253166.1:n.*209_*212del
XM_011520344.2:c.*209_*212del (TUB) XP_011518646.1:n.*209_*212del
XR_001747957.2:n.1335-7672_1335-7669del (RIC3)
XR_428851.4:n.1422-7672_1422-7669del (RIC3)
XR_930896.3:n.1484+5504_1484+5507del (RIC3)
XR_930900.3:n.1485-4109_1485-4106del (RIC3)
NM_177972.3:c.*209_*212del (TUB) MANE Select NP_813977.1:n.*209_*212del
NR_144485.2:n.1450+5504_1450+5507del (RIC3)
NM_003320.5:c.*209_*212del (TUB) NP_003311.2:n.*209_*212del