Canonical Allele Identifier: CA1310555923
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630312C= , CM000664.2:g.178630312C= GRCh38
NC_000002.11:g.179495039C= , CM000664.1:g.179495039C= GRCh37
NC_000002.10:g.179203284C= NCBI36
NG_011618.3:g.205491G= , LRG_391:g.205491G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36506G= ENSP00000343764.6:p.Arg12169=
ENST00000342175.11:c.17591G= ENSP00000340554.6:p.Arg5864=
ENST00000359218.10:c.17390G= ENSP00000352154.5:p.Arg5797=
ENST00000342175.10:c.17591G= ENSP00000340554.6:p.Arg5864=
ENST00000342992.10:c.36506G= ENSP00000343764.6:p.Arg12169=
ENST00000359218.9:c.17390G= ENSP00000352154.5:p.Arg5797=
ENST00000460472.6:c.17015G= ENSP00000434586.1:p.Arg5672=
ENST00000589042.5:c.44210G= MANE Select ENSP00000467141.1:p.Arg14737=
ENST00000591111.5:c.39287G= ENSP00000465570.1:p.Arg13096=
ENST00000615779.4:c.39287G= ENSP00000483597.1:p.Arg13096=
NM_001256850.1:c.39287G= NP_001243779.1:p.Arg13096=
NM_001267550.2:c.44210G= MANE Select NP_001254479.2:p.Arg14737=
NM_003319.4:c.17015G= NP_003310.4:p.Arg5672=
NM_133378.4:c.36506G= NP_596869.4:p.Arg12169=
NM_133432.3:c.17390G= NP_597676.3:p.Arg5797=
NM_133437.4:c.17591G= NP_597681.4:p.Arg5864=
XM_011511729.1:c.43307G= XP_011510031.1:p.Arg14436=
XM_011511730.1:c.17201G= XP_011510032.1:p.Arg5734=
XM_011511731.1:c.17060G= XP_011510033.1:p.Arg5687=
XM_017004819.1:c.43103G= XP_016860308.1:p.Arg14368=
XM_017004820.1:c.38501G= XP_016860309.1:p.Arg12834=
XM_017004821.1:c.38498G= XP_016860310.1:p.Arg12833=
XM_017004822.1:c.35540G= XP_016860311.1:p.Arg11847=
XM_017004823.1:c.17156G= XP_016860312.1:p.Arg5719=
XM_024453094.1:c.38651G= XP_024308862.1:p.Arg12884=
XM_024453095.1:c.38648G= XP_024308863.1:p.Arg12883=
XM_024453096.1:c.38081G= XP_024308864.1:p.Arg12694=
XM_024453097.1:c.35423G= XP_024308865.1:p.Arg11808=
XM_024453098.1:c.35342G= XP_024308866.1:p.Arg11781=
XM_024453099.1:c.17105G= XP_024308867.1:p.Arg5702=
XM_024453100.1:c.6959G= XP_024308868.1:p.Arg2320=