Canonical Allele Identifier: CA1310511374

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530046G= , CM000664.2:g.178530046G= GRCh38
NC_000002.11:g.179394773G= , CM000664.1:g.179394773G= GRCh37
NC_000002.10:g.179103019G= NCBI36
NG_011618.3:g.305757C= , LRG_391:g.305757C=
NG_051363.1:g.12220G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98741C= (TTN) ENSP00000343764.6:p.Thr32914=
ENST00000342175.11:c.79826C= (TTN) ENSP00000340554.6:p.Thr26609=
ENST00000359218.10:c.79625C= (TTN) ENSP00000352154.5:p.Thr26542=
ENST00000342175.10:c.79826C= (TTN) ENSP00000340554.6:p.Thr26609=
ENST00000342992.10:c.98741C= (TTN) ENSP00000343764.6:p.Thr32914=
ENST00000359218.9:c.79625C= (TTN) ENSP00000352154.5:p.Thr26542=
ENST00000460472.6:c.79250C= (TTN) ENSP00000434586.1:p.Thr26417=
ENST00000589042.5:c.106445C= (TTN) MANE Select ENSP00000467141.1:p.Thr35482=
ENST00000591111.5:c.101522C= (TTN) ENSP00000465570.1:p.Thr33841=
ENST00000615779.4:c.101522C= (TTN) ENSP00000483597.1:p.Thr33841=
NM_001256850.1:c.101522C= (TTN) NP_001243779.1:p.Thr33841=
NM_001267550.2:c.106445C= (TTN) MANE Select NP_001254479.2:p.Thr35482=
NM_003319.4:c.79250C= (TTN) NP_003310.4:p.Thr26417=
NM_133378.4:c.98741C= (TTN) NP_596869.4:p.Thr32914=
NM_133432.3:c.79625C= (TTN) NP_597676.3:p.Thr26542=
NM_133437.4:c.79826C= (TTN) NP_597681.4:p.Thr26609=
NR_038271.1:n.446+6410G= (TTN-AS1)
NR_038272.1:n.220-5686G= (TTN-AS1)
XM_011511729.1:c.105542C= (TTN) XP_011510031.1:p.Thr35181=
XM_011511730.1:c.79436C= (TTN) XP_011510032.1:p.Thr26479=
XM_011511731.1:c.79295C= (TTN) XP_011510033.1:p.Thr26432=
XM_017004819.1:c.105338C= (TTN) XP_016860308.1:p.Thr35113=
XM_017004820.1:c.100736C= (TTN) XP_016860309.1:p.Thr33579=
XM_017004821.1:c.100733C= (TTN) XP_016860310.1:p.Thr33578=
XM_017004822.1:c.97775C= (TTN) XP_016860311.1:p.Thr32592=
XM_017004823.1:c.79391C= (TTN) XP_016860312.1:p.Thr26464=
XM_024453094.1:c.100886C= (TTN) XP_024308862.1:p.Thr33629=
XM_024453095.1:c.100883C= (TTN) XP_024308863.1:p.Thr33628=
XM_024453096.1:c.100316C= (TTN) XP_024308864.1:p.Thr33439=
XM_024453097.1:c.97658C= (TTN) XP_024308865.1:p.Thr32553=
XM_024453098.1:c.97577C= (TTN) XP_024308866.1:p.Thr32526=
XM_024453099.1:c.79340C= (TTN) XP_024308867.1:p.Thr26447=
XM_024453100.1:c.69194C= (TTN) XP_024308868.1:p.Thr23065=