Canonical Allele Identifier: CA2574746063

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8101697T>A , CM000673.2:g.8101697T>A GRCh38
NC_000011.9:g.8123244T>A , CM000673.1:g.8123244T>A GRCh37
NC_000011.8:g.8079820T>A NCBI36
NG_029912.1:g.68065T>A
NG_030416.2:g.72347A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.*78T>A (TUB) MANE Select ENSP00000299506.3:n.*78T>A
ENST00000299506.2:c.*78T>A (TUB) ENSP00000299506.2:n.*78T>A
ENST00000305253.8:c.*78T>A (TUB) ENSP00000305426.4:n.*78T>A
ENST00000534099.5:c.*78T>A (TUB) ENSP00000434400.1:n.*78T>A
NM_003320.4:c.*78T>A (TUB) NP_003311.2:n.*78T>A
NM_177972.2:c.*78T>A (TUB) NP_813977.1:n.*78T>A
XM_005253109.2:c.*78T>A (TUB) XP_005253166.1:n.*78T>A
XM_011520344.1:c.*78T>A (TUB) XP_011518646.1:n.*78T>A
XR_428851.2:n.1484-7538A>T (RIC3)
XR_930896.1:n.1546+5638A>T (RIC3)
XR_930900.1:n.1547-3975A>T (RIC3)
NR_144485.1:n.1519+5638A>T (RIC3)
XM_005253109.3:c.*78T>A (TUB) XP_005253166.1:n.*78T>A
XM_011520344.2:c.*78T>A (TUB) XP_011518646.1:n.*78T>A
XR_001747957.2:n.1335-7538A>T (RIC3)
XR_428851.4:n.1422-7538A>T (RIC3)
XR_930896.3:n.1484+5638A>T (RIC3)
XR_930900.3:n.1485-3975A>T (RIC3)
NM_177972.3:c.*78T>A (TUB) MANE Select NP_813977.1:n.*78T>A
NR_144485.2:n.1450+5638A>T (RIC3)
NM_003320.5:c.*78T>A (TUB) NP_003311.2:n.*78T>A