Canonical Allele Identifier: CA2612334428

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101856_8101857del , CM000673.2:g.8101856_8101857del GRCh38
NC_000011.9:g.8123403_8123404del , CM000673.1:g.8123403_8123404del GRCh37
NC_000011.8:g.8079979_8079980del NCBI36
NG_029912.1:g.68224_68225del
NG_030416.2:g.72187_72188del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*237_*238del (TUB) MANE Select ENSP00000299506.3:n.*237_*238del
ENST00000299506.2:c.*237_*238del (TUB) ENSP00000299506.2:n.*237_*238del
ENST00000305253.8:c.*237_*238del (TUB) ENSP00000305426.4:n.*237_*238del
NM_003320.4:c.*237_*238del (TUB) NP_003311.2:n.*237_*238del
NM_177972.2:c.*237_*238del (TUB) NP_813977.1:n.*237_*238del
XM_005253109.2:c.*237_*238del (TUB) XP_005253166.1:n.*237_*238del
XM_011520344.1:c.*237_*238del (TUB) XP_011518646.1:n.*237_*238del
XR_428851.2:n.1484-7698_1484-7697del (RIC3)
XR_930896.1:n.1546+5478_1546+5479del (RIC3)
XR_930900.1:n.1547-4135_1547-4134del (RIC3)
NR_144485.1:n.1519+5478_1519+5479del (RIC3)
XM_005253109.3:c.*237_*238del (TUB) XP_005253166.1:n.*237_*238del
XM_011520344.2:c.*237_*238del (TUB) XP_011518646.1:n.*237_*238del
XR_001747957.2:n.1335-7698_1335-7697del (RIC3)
XR_428851.4:n.1422-7698_1422-7697del (RIC3)
XR_930896.3:n.1484+5478_1484+5479del (RIC3)
XR_930900.3:n.1485-4135_1485-4134del (RIC3)
NM_177972.3:c.*237_*238del (TUB) MANE Select NP_813977.1:n.*237_*238del
NR_144485.2:n.1450+5478_1450+5479del (RIC3)
NM_003320.5:c.*237_*238del (TUB) NP_003311.2:n.*237_*238del