Canonical Allele Identifier: CA1310520605

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543266C= , CM000664.2:g.178543266C= GRCh38
NC_000002.11:g.179407993C= , CM000664.1:g.179407993C= GRCh37
NC_000002.10:g.179116239C= NCBI36
NG_011618.3:g.292537G= , LRG_391:g.292537G=
NG_051363.1:g.25440C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.89003G= (TTN) ENSP00000343764.6:p.Gly29668=
ENST00000342175.11:c.70088G= (TTN) ENSP00000340554.6:p.Gly23363=
ENST00000359218.10:c.69887G= (TTN) ENSP00000352154.5:p.Gly23296=
ENST00000342175.10:c.70088G= (TTN) ENSP00000340554.6:p.Gly23363=
ENST00000342992.10:c.89003G= (TTN) ENSP00000343764.6:p.Gly29668=
ENST00000359218.9:c.69887G= (TTN) ENSP00000352154.5:p.Gly23296=
ENST00000460472.6:c.69512G= (TTN) ENSP00000434586.1:p.Gly23171=
ENST00000589042.5:c.96707G= (TTN) MANE Select ENSP00000467141.1:p.Gly32236=
ENST00000591111.5:c.91784G= (TTN) ENSP00000465570.1:p.Gly30595=
ENST00000615779.4:c.91784G= (TTN) ENSP00000483597.1:p.Gly30595=
NM_001256850.1:c.91784G= (TTN) NP_001243779.1:p.Gly30595=
NM_001267550.2:c.96707G= (TTN) MANE Select NP_001254479.2:p.Gly32236=
NM_003319.4:c.69512G= (TTN) NP_003310.4:p.Gly23171=
NM_133378.4:c.89003G= (TTN) NP_596869.4:p.Gly29668=
NM_133432.3:c.69887G= (TTN) NP_597676.3:p.Gly23296=
NM_133437.4:c.70088G= (TTN) NP_597681.4:p.Gly23363=
NR_038271.1:n.446+19630C= (TTN-AS1)
NR_038272.1:n.2043+905C= (TTN-AS1)
XM_011511729.1:c.95804G= (TTN) XP_011510031.1:p.Gly31935=
XM_011511730.1:c.69698G= (TTN) XP_011510032.1:p.Gly23233=
XM_011511731.1:c.69557G= (TTN) XP_011510033.1:p.Gly23186=
XM_017004819.1:c.95600G= (TTN) XP_016860308.1:p.Gly31867=
XM_017004820.1:c.90998G= (TTN) XP_016860309.1:p.Gly30333=
XM_017004821.1:c.90995G= (TTN) XP_016860310.1:p.Gly30332=
XM_017004822.1:c.88037G= (TTN) XP_016860311.1:p.Gly29346=
XM_017004823.1:c.69653G= (TTN) XP_016860312.1:p.Gly23218=
XM_024453094.1:c.91148G= (TTN) XP_024308862.1:p.Gly30383=
XM_024453095.1:c.91145G= (TTN) XP_024308863.1:p.Gly30382=
XM_024453096.1:c.90578G= (TTN) XP_024308864.1:p.Gly30193=
XM_024453097.1:c.87920G= (TTN) XP_024308865.1:p.Gly29307=
XM_024453098.1:c.87839G= (TTN) XP_024308866.1:p.Gly29280=
XM_024453099.1:c.69602G= (TTN) XP_024308867.1:p.Gly23201=
XM_024453100.1:c.59456G= (TTN) XP_024308868.1:p.Gly19819=