Canonical Allele Identifier: CA1950967997

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101627T= , CM000673.2:g.8101627T= GRCh38
NC_000011.9:g.8123174T= , CM000673.1:g.8123174T= GRCh37
NC_000011.8:g.8079750T= NCBI36
NG_029912.1:g.67995T=
NG_030416.2:g.72417A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*8T= (TUB) MANE Select ENSP00000299506.3:n.*8T=
ENST00000299506.2:c.*8T= (TUB) ENSP00000299506.2:n.*8T=
ENST00000305253.8:c.*8T= (TUB) ENSP00000305426.4:n.*8T=
ENST00000534099.5:c.*8T= (TUB) ENSP00000434400.1:n.*8T=
NM_003320.4:c.*8T= (TUB) NP_003311.2:n.*8T=
NM_177972.2:c.*8T= (TUB) NP_813977.1:n.*8T=
XM_005253109.2:c.*8T= (TUB) XP_005253166.1:n.*8T=
XM_011520344.1:c.*8T= (TUB) XP_011518646.1:n.*8T=
XR_428851.2:n.1484-7468A= (RIC3)
XR_930896.1:n.1546+5708A= (RIC3)
XR_930900.1:n.1547-3905A= (RIC3)
NR_144485.1:n.1519+5708A= (RIC3)
XM_005253109.3:c.*8T= (TUB) XP_005253166.1:n.*8T=
XM_011520344.2:c.*8T= (TUB) XP_011518646.1:n.*8T=
XR_001747957.2:n.1335-7468A= (RIC3)
XR_428851.4:n.1422-7468A= (RIC3)
XR_930896.3:n.1484+5708A= (RIC3)
XR_930900.3:n.1485-3905A= (RIC3)
NM_177972.3:c.*8T= (TUB) MANE Select NP_813977.1:n.*8T=
NR_144485.2:n.1450+5708A= (RIC3)
NM_003320.5:c.*8T= (TUB) NP_003311.2:n.*8T=