Canonical Allele Identifier: CA1310553526
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178624499C= , CM000664.2:g.178624499C= GRCh38
NC_000002.11:g.179489226C= , CM000664.1:g.179489226C= GRCh37
NC_000002.10:g.179197471C= NCBI36
NG_011618.3:g.211304G= , LRG_391:g.211304G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.37077G= ENSP00000343764.6:p.Lys12359=
ENST00000342175.11:c.18162G= ENSP00000340554.6:p.Lys6054=
ENST00000359218.10:c.17961G= ENSP00000352154.5:p.Lys5987=
ENST00000342175.10:c.18162G= ENSP00000340554.6:p.Lys6054=
ENST00000342992.10:c.37077G= ENSP00000343764.6:p.Lys12359=
ENST00000359218.9:c.17961G= ENSP00000352154.5:p.Lys5987=
ENST00000460472.6:c.17586G= ENSP00000434586.1:p.Lys5862=
ENST00000589042.5:c.44781G= MANE Select ENSP00000467141.1:p.Lys14927=
ENST00000591111.5:c.39858G= ENSP00000465570.1:p.Lys13286=
ENST00000615779.4:c.39858G= ENSP00000483597.1:p.Lys13286=
NM_001256850.1:c.39858G= NP_001243779.1:p.Lys13286=
NM_001267550.2:c.44781G= MANE Select NP_001254479.2:p.Lys14927=
NM_003319.4:c.17586G= NP_003310.4:p.Lys5862=
NM_133378.4:c.37077G= NP_596869.4:p.Lys12359=
NM_133432.3:c.17961G= NP_597676.3:p.Lys5987=
NM_133437.4:c.18162G= NP_597681.4:p.Lys6054=
XM_011511729.1:c.43878G= XP_011510031.1:p.Lys14626=
XM_011511730.1:c.17772G= XP_011510032.1:p.Lys5924=
XM_011511731.1:c.17631G= XP_011510033.1:p.Lys5877=
XM_017004819.1:c.43674G= XP_016860308.1:p.Lys14558=
XM_017004820.1:c.39072G= XP_016860309.1:p.Lys13024=
XM_017004821.1:c.39069G= XP_016860310.1:p.Lys13023=
XM_017004822.1:c.36111G= XP_016860311.1:p.Lys12037=
XM_017004823.1:c.17727G= XP_016860312.1:p.Lys5909=
XM_024453094.1:c.39222G= XP_024308862.1:p.Lys13074=
XM_024453095.1:c.39219G= XP_024308863.1:p.Lys13073=
XM_024453096.1:c.38652G= XP_024308864.1:p.Lys12884=
XM_024453097.1:c.35994G= XP_024308865.1:p.Lys11998=
XM_024453098.1:c.35913G= XP_024308866.1:p.Lys11971=
XM_024453099.1:c.17676G= XP_024308867.1:p.Lys5892=
XM_024453100.1:c.7530G= XP_024308868.1:p.Lys2510=