Canonical Allele Identifier: CA1310556249
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631170C= , CM000664.2:g.178631170C= GRCh38
NC_000002.11:g.179495897C= , CM000664.1:g.179495897C= GRCh37
NC_000002.10:g.179204142C= NCBI36
NG_011618.3:g.204633G= , LRG_391:g.204633G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36174G= ENSP00000343764.6:p.Lys12058=
ENST00000342175.11:c.17259G= ENSP00000340554.6:p.Lys5753=
ENST00000359218.10:c.17058G= ENSP00000352154.5:p.Lys5686=
ENST00000342175.10:c.17259G= ENSP00000340554.6:p.Lys5753=
ENST00000342992.10:c.36174G= ENSP00000343764.6:p.Lys12058=
ENST00000359218.9:c.17058G= ENSP00000352154.5:p.Lys5686=
ENST00000460472.6:c.16683G= ENSP00000434586.1:p.Lys5561=
ENST00000589042.5:c.43878G= MANE Select ENSP00000467141.1:p.Lys14626=
ENST00000591111.5:c.38955G= ENSP00000465570.1:p.Lys12985=
ENST00000615779.4:c.38955G= ENSP00000483597.1:p.Lys12985=
NM_001256850.1:c.38955G= NP_001243779.1:p.Lys12985=
NM_001267550.2:c.43878G= MANE Select NP_001254479.2:p.Lys14626=
NM_003319.4:c.16683G= NP_003310.4:p.Lys5561=
NM_133378.4:c.36174G= NP_596869.4:p.Lys12058=
NM_133432.3:c.17058G= NP_597676.3:p.Lys5686=
NM_133437.4:c.17259G= NP_597681.4:p.Lys5753=
XM_011511729.1:c.42975G= XP_011510031.1:p.Lys14325=
XM_011511730.1:c.16869G= XP_011510032.1:p.Lys5623=
XM_011511731.1:c.16728G= XP_011510033.1:p.Lys5576=
XM_017004819.1:c.42771G= XP_016860308.1:p.Lys14257=
XM_017004820.1:c.38169G= XP_016860309.1:p.Lys12723=
XM_017004821.1:c.38166G= XP_016860310.1:p.Lys12722=
XM_017004822.1:c.35208G= XP_016860311.1:p.Lys11736=
XM_017004823.1:c.16824G= XP_016860312.1:p.Lys5608=
XM_024453094.1:c.38319G= XP_024308862.1:p.Lys12773=
XM_024453095.1:c.38316G= XP_024308863.1:p.Lys12772=
XM_024453096.1:c.37749G= XP_024308864.1:p.Lys12583=
XM_024453097.1:c.35091G= XP_024308865.1:p.Lys11697=
XM_024453098.1:c.35010G= XP_024308866.1:p.Lys11670=
XM_024453099.1:c.16773G= XP_024308867.1:p.Lys5591=
XM_024453100.1:c.6627G= XP_024308868.1:p.Lys2209=