Canonical Allele Identifier: CA1950968130

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101721A= , CM000673.2:g.8101721A= GRCh38
NC_000011.9:g.8123268A= , CM000673.1:g.8123268A= GRCh37
NC_000011.8:g.8079844A= NCBI36
NG_029912.1:g.68089A=
NG_030416.2:g.72323T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*102A= (TUB) MANE Select ENSP00000299506.3:n.*102A=
ENST00000299506.2:c.*102A= (TUB) ENSP00000299506.2:n.*102A=
ENST00000305253.8:c.*102A= (TUB) ENSP00000305426.4:n.*102A=
ENST00000534099.5:c.*102A= (TUB) ENSP00000434400.1:n.*102A=
NM_003320.4:c.*102A= (TUB) NP_003311.2:n.*102A=
NM_177972.2:c.*102A= (TUB) NP_813977.1:n.*102A=
XM_005253109.2:c.*102A= (TUB) XP_005253166.1:n.*102A=
XM_011520344.1:c.*102A= (TUB) XP_011518646.1:n.*102A=
XR_428851.2:n.1484-7562T= (RIC3)
XR_930896.1:n.1546+5614T= (RIC3)
XR_930900.1:n.1547-3999T= (RIC3)
NR_144485.1:n.1519+5614T= (RIC3)
XM_005253109.3:c.*102A= (TUB) XP_005253166.1:n.*102A=
XM_011520344.2:c.*102A= (TUB) XP_011518646.1:n.*102A=
XR_001747957.2:n.1335-7562T= (RIC3)
XR_428851.4:n.1422-7562T= (RIC3)
XR_930896.3:n.1484+5614T= (RIC3)
XR_930900.3:n.1485-3999T= (RIC3)
NM_177972.3:c.*102A= (TUB) MANE Select NP_813977.1:n.*102A=
NR_144485.2:n.1450+5614T= (RIC3)
NM_003320.5:c.*102A= (TUB) NP_003311.2:n.*102A=