Canonical Allele Identifier: CA1310555924
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630313G= , CM000664.2:g.178630313G= GRCh38
NC_000002.11:g.179495040G= , CM000664.1:g.179495040G= GRCh37
NC_000002.10:g.179203285G= NCBI36
NG_011618.3:g.205490C= , LRG_391:g.205490C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36505C= ENSP00000343764.6:p.Arg12169=
ENST00000342175.11:c.17590C= ENSP00000340554.6:p.Arg5864=
ENST00000359218.10:c.17389C= ENSP00000352154.5:p.Arg5797=
ENST00000342175.10:c.17590C= ENSP00000340554.6:p.Arg5864=
ENST00000342992.10:c.36505C= ENSP00000343764.6:p.Arg12169=
ENST00000359218.9:c.17389C= ENSP00000352154.5:p.Arg5797=
ENST00000460472.6:c.17014C= ENSP00000434586.1:p.Arg5672=
ENST00000589042.5:c.44209C= MANE Select ENSP00000467141.1:p.Arg14737=
ENST00000591111.5:c.39286C= ENSP00000465570.1:p.Arg13096=
ENST00000615779.4:c.39286C= ENSP00000483597.1:p.Arg13096=
NM_001256850.1:c.39286C= NP_001243779.1:p.Arg13096=
NM_001267550.2:c.44209C= MANE Select NP_001254479.2:p.Arg14737=
NM_003319.4:c.17014C= NP_003310.4:p.Arg5672=
NM_133378.4:c.36505C= NP_596869.4:p.Arg12169=
NM_133432.3:c.17389C= NP_597676.3:p.Arg5797=
NM_133437.4:c.17590C= NP_597681.4:p.Arg5864=
XM_011511729.1:c.43306C= XP_011510031.1:p.Arg14436=
XM_011511730.1:c.17200C= XP_011510032.1:p.Arg5734=
XM_011511731.1:c.17059C= XP_011510033.1:p.Arg5687=
XM_017004819.1:c.43102C= XP_016860308.1:p.Arg14368=
XM_017004820.1:c.38500C= XP_016860309.1:p.Arg12834=
XM_017004821.1:c.38497C= XP_016860310.1:p.Arg12833=
XM_017004822.1:c.35539C= XP_016860311.1:p.Arg11847=
XM_017004823.1:c.17155C= XP_016860312.1:p.Arg5719=
XM_024453094.1:c.38650C= XP_024308862.1:p.Arg12884=
XM_024453095.1:c.38647C= XP_024308863.1:p.Arg12883=
XM_024453096.1:c.38080C= XP_024308864.1:p.Arg12694=
XM_024453097.1:c.35422C= XP_024308865.1:p.Arg11808=
XM_024453098.1:c.35341C= XP_024308866.1:p.Arg11781=
XM_024453099.1:c.17104C= XP_024308867.1:p.Arg5702=
XM_024453100.1:c.6958C= XP_024308868.1:p.Arg2320=