Canonical Allele Identifier: CA2612334421

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101855_8101856del , CM000673.2:g.8101855_8101856del GRCh38
NC_000011.9:g.8123402_8123403del , CM000673.1:g.8123402_8123403del GRCh37
NC_000011.8:g.8079978_8079979del NCBI36
NG_029912.1:g.68223_68224del
NG_030416.2:g.72188_72189del

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.*236_*237del (TUB) MANE Select ENSP00000299506.3:n.*236_*237del
ENST00000299506.2:c.*236_*237del (TUB) ENSP00000299506.2:n.*236_*237del
ENST00000305253.8:c.*236_*237del (TUB) ENSP00000305426.4:n.*236_*237del
NM_003320.4:c.*236_*237del (TUB) NP_003311.2:n.*236_*237del
NM_177972.2:c.*236_*237del (TUB) NP_813977.1:n.*236_*237del
XM_005253109.2:c.*236_*237del (TUB) XP_005253166.1:n.*236_*237del
XM_011520344.1:c.*236_*237del (TUB) XP_011518646.1:n.*236_*237del
XR_428851.2:n.1484-7697_1484-7696del (RIC3)
XR_930896.1:n.1546+5479_1546+5480del (RIC3)
XR_930900.1:n.1547-4134_1547-4133del (RIC3)
NR_144485.1:n.1519+5479_1519+5480del (RIC3)
XM_005253109.3:c.*236_*237del (TUB) XP_005253166.1:n.*236_*237del
XM_011520344.2:c.*236_*237del (TUB) XP_011518646.1:n.*236_*237del
XR_001747957.2:n.1335-7697_1335-7696del (RIC3)
XR_428851.4:n.1422-7697_1422-7696del (RIC3)
XR_930896.3:n.1484+5479_1484+5480del (RIC3)
XR_930900.3:n.1485-4134_1485-4133del (RIC3)
NM_177972.3:c.*236_*237del (TUB) MANE Select NP_813977.1:n.*236_*237del
NR_144485.2:n.1450+5479_1450+5480del (RIC3)
NM_003320.5:c.*236_*237del (TUB) NP_003311.2:n.*236_*237del