Canonical Allele Identifier: CA1310580093
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178689134G= , CM000664.2:g.178689134G= GRCh38
NC_000002.11:g.179553861G= , CM000664.1:g.179553861G= GRCh37
NC_000002.10:g.179262106G= NCBI36
NG_011618.3:g.146669C= , LRG_391:g.146669C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.28282C= ENSP00000343764.6:p.Pro9428=
ENST00000342175.11:c.13859-46817C= ENSP00000340554.6:n.13859-46817C=
ENST00000359218.10:c.13658-46817C= ENSP00000352154.5:n.13658-46817C=
ENST00000342175.10:c.13859-46817C= ENSP00000340554.6:n.13859-46817C=
ENST00000342992.10:c.28282C= ENSP00000343764.6:p.Pro9428=
ENST00000359218.9:c.13658-46817C= ENSP00000352154.5:n.13658-46817C=
ENST00000414766.5:c.1648C= ENSP00000401501.1:p.Pro550=
ENST00000460472.6:c.13283-46817C= ENSP00000434586.1:n.13283-46817C=
ENST00000589042.5:c.32014C= MANE Select ENSP00000467141.1:p.Pro10672=
ENST00000591111.5:c.31063C= ENSP00000465570.1:p.Pro10355=
ENST00000615779.4:c.31063C= ENSP00000483597.1:p.Pro10355=
NM_001256850.1:c.31063C= NP_001243779.1:p.Pro10355=
NM_001267550.2:c.32014C= MANE Select NP_001254479.2:p.Pro10672=
NM_003319.4:c.13283-46817C= NP_003310.4:n.13283-46817C=
NM_133378.4:c.28282C= NP_596869.4:p.Pro9428=
NM_133432.3:c.13658-46817C= NP_597676.3:n.13658-46817C=
NM_133437.4:c.13859-46817C= NP_597681.4:n.13859-46817C=
XM_011511729.1:c.31111C= XP_011510031.1:p.Pro10371=
XM_011511730.1:c.13469-46817C= XP_011510032.1:n.13469-46817C=
XM_011511731.1:c.13328-46817C= XP_011510033.1:n.13328-46817C=
XM_017004819.1:c.31066C= XP_016860308.1:p.Pro10356=
XM_017004820.1:c.28285C= XP_016860309.1:p.Pro9429=
XM_017004821.1:c.28282C= XP_016860310.1:p.Pro9428=
XM_017004822.1:c.31066C= XP_016860311.1:p.Pro10356=
XM_017004823.1:c.13424-46817C= XP_016860312.1:n.13424-46817C=
XM_024453094.1:c.31066C= XP_024308862.1:p.Pro10356=
XM_024453095.1:c.31066C= XP_024308863.1:p.Pro10356=
XM_024453096.1:c.31066C= XP_024308864.1:p.Pro10356=
XM_024453097.1:c.30898+679C= XP_024308865.1:n.30898+679C=
XM_024453098.1:c.30898+679C= XP_024308866.1:n.30898+679C=
XM_024453099.1:c.13424-46817C= XP_024308867.1:n.13424-46817C=