Canonical Allele Identifier: CA1310553444
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178624326G= , CM000664.2:g.178624326G= GRCh38
NC_000002.11:g.179489053G= , CM000664.1:g.179489053G= GRCh37
NC_000002.10:g.179197298G= NCBI36
NG_011618.3:g.211477C= , LRG_391:g.211477C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.37111+139C= ENSP00000343764.6:n.37111+139C=
ENST00000342175.11:c.18196+139C= ENSP00000340554.6:n.18196+139C=
ENST00000359218.10:c.17995+139C= ENSP00000352154.5:n.17995+139C=
ENST00000342175.10:c.18196+139C= ENSP00000340554.6:n.18196+139C=
ENST00000342992.10:c.37111+139C= ENSP00000343764.6:n.37111+139C=
ENST00000359218.9:c.17995+139C= ENSP00000352154.5:n.17995+139C=
ENST00000460472.6:c.17620+139C= ENSP00000434586.1:n.17620+139C=
ENST00000589042.5:c.44815+139C= MANE Select ENSP00000467141.1:n.44815+139C=
ENST00000591111.5:c.39892+139C= ENSP00000465570.1:n.39892+139C=
ENST00000615779.4:c.39892+139C= ENSP00000483597.1:n.39892+139C=
NM_001256850.1:c.39892+139C= NP_001243779.1:n.39892+139C=
NM_001267550.2:c.44815+139C= MANE Select NP_001254479.2:n.44815+139C=
NM_003319.4:c.17620+139C= NP_003310.4:n.17620+139C=
NM_133378.4:c.37111+139C= NP_596869.4:n.37111+139C=
NM_133432.3:c.17995+139C= NP_597676.3:n.17995+139C=
NM_133437.4:c.18196+139C= NP_597681.4:n.18196+139C=
XM_011511729.1:c.43912+139C= XP_011510031.1:n.43912+139C=
XM_011511730.1:c.17806+139C= XP_011510032.1:n.17806+139C=
XM_011511731.1:c.17665+139C= XP_011510033.1:n.17665+139C=
XM_017004819.1:c.43708+139C= XP_016860308.1:n.43708+139C=
XM_017004820.1:c.39106+139C= XP_016860309.1:n.39106+139C=
XM_017004821.1:c.39103+139C= XP_016860310.1:n.39103+139C=
XM_017004822.1:c.36145+139C= XP_016860311.1:n.36145+139C=
XM_017004823.1:c.17761+139C= XP_016860312.1:n.17761+139C=
XM_024453094.1:c.39256+139C= XP_024308862.1:n.39256+139C=
XM_024453095.1:c.39253+139C= XP_024308863.1:n.39253+139C=
XM_024453096.1:c.38686+139C= XP_024308864.1:n.38686+139C=
XM_024453097.1:c.36028+139C= XP_024308865.1:n.36028+139C=
XM_024453098.1:c.35947+139C= XP_024308866.1:n.35947+139C=
XM_024453099.1:c.17710+139C= XP_024308867.1:n.17710+139C=
XM_024453100.1:c.7564+139C= XP_024308868.1:n.7564+139C=