Canonical Allele Identifier: CA1310514761

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530566G= , CM000664.2:g.178530566G= GRCh38
NC_000002.11:g.179395293G= , CM000664.1:g.179395293G= GRCh37
NC_000002.10:g.179103539G= NCBI36
NG_011618.3:g.305237C= , LRG_391:g.305237C=
NG_051363.1:g.12740G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98345C= (TTN) ENSP00000343764.6:p.Thr32782=
ENST00000342175.11:c.79430C= (TTN) ENSP00000340554.6:p.Thr26477=
ENST00000359218.10:c.79229C= (TTN) ENSP00000352154.5:p.Thr26410=
ENST00000342175.10:c.79430C= (TTN) ENSP00000340554.6:p.Thr26477=
ENST00000342992.10:c.98345C= (TTN) ENSP00000343764.6:p.Thr32782=
ENST00000359218.9:c.79229C= (TTN) ENSP00000352154.5:p.Thr26410=
ENST00000460472.6:c.78854C= (TTN) ENSP00000434586.1:p.Thr26285=
ENST00000589042.5:c.106049C= (TTN) MANE Select ENSP00000467141.1:p.Thr35350=
ENST00000591111.5:c.101126C= (TTN) ENSP00000465570.1:p.Thr33709=
ENST00000615779.4:c.101126C= (TTN) ENSP00000483597.1:p.Thr33709=
NM_001256850.1:c.101126C= (TTN) NP_001243779.1:p.Thr33709=
NM_001267550.2:c.106049C= (TTN) MANE Select NP_001254479.2:p.Thr35350=
NM_003319.4:c.78854C= (TTN) NP_003310.4:p.Thr26285=
NM_133378.4:c.98345C= (TTN) NP_596869.4:p.Thr32782=
NM_133432.3:c.79229C= (TTN) NP_597676.3:p.Thr26410=
NM_133437.4:c.79430C= (TTN) NP_597681.4:p.Thr26477=
NR_038271.1:n.446+6930G= (TTN-AS1)
NR_038272.1:n.220-5166G= (TTN-AS1)
XM_011511729.1:c.105146C= (TTN) XP_011510031.1:p.Thr35049=
XM_011511730.1:c.79040C= (TTN) XP_011510032.1:p.Thr26347=
XM_011511731.1:c.78899C= (TTN) XP_011510033.1:p.Thr26300=
XM_017004819.1:c.104942C= (TTN) XP_016860308.1:p.Thr34981=
XM_017004820.1:c.100340C= (TTN) XP_016860309.1:p.Thr33447=
XM_017004821.1:c.100337C= (TTN) XP_016860310.1:p.Thr33446=
XM_017004822.1:c.97379C= (TTN) XP_016860311.1:p.Thr32460=
XM_017004823.1:c.78995C= (TTN) XP_016860312.1:p.Thr26332=
XM_024453094.1:c.100490C= (TTN) XP_024308862.1:p.Thr33497=
XM_024453095.1:c.100487C= (TTN) XP_024308863.1:p.Thr33496=
XM_024453096.1:c.99920C= (TTN) XP_024308864.1:p.Thr33307=
XM_024453097.1:c.97262C= (TTN) XP_024308865.1:p.Thr32421=
XM_024453098.1:c.97181C= (TTN) XP_024308866.1:p.Thr32394=
XM_024453099.1:c.78944C= (TTN) XP_024308867.1:p.Thr26315=
XM_024453100.1:c.68798C= (TTN) XP_024308868.1:p.Thr22933=