Canonical Allele Identifier: CA1310555845
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630142A= , CM000664.2:g.178630142A= GRCh38
NC_000002.11:g.179494869A= , CM000664.1:g.179494869A= GRCh37
NC_000002.10:g.179203114A= NCBI36
NG_011618.3:g.205661T= , LRG_391:g.205661T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36577+99T= ENSP00000343764.6:n.36577+99T=
ENST00000342175.11:c.17662+99T= ENSP00000340554.6:n.17662+99T=
ENST00000359218.10:c.17461+99T= ENSP00000352154.5:n.17461+99T=
ENST00000342175.10:c.17662+99T= ENSP00000340554.6:n.17662+99T=
ENST00000342992.10:c.36577+99T= ENSP00000343764.6:n.36577+99T=
ENST00000359218.9:c.17461+99T= ENSP00000352154.5:n.17461+99T=
ENST00000460472.6:c.17086+99T= ENSP00000434586.1:n.17086+99T=
ENST00000589042.5:c.44281+99T= MANE Select ENSP00000467141.1:n.44281+99T=
ENST00000591111.5:c.39358+99T= ENSP00000465570.1:n.39358+99T=
ENST00000615779.4:c.39358+99T= ENSP00000483597.1:n.39358+99T=
NM_001256850.1:c.39358+99T= NP_001243779.1:n.39358+99T=
NM_001267550.2:c.44281+99T= MANE Select NP_001254479.2:n.44281+99T=
NM_003319.4:c.17086+99T= NP_003310.4:n.17086+99T=
NM_133378.4:c.36577+99T= NP_596869.4:n.36577+99T=
NM_133432.3:c.17461+99T= NP_597676.3:n.17461+99T=
NM_133437.4:c.17662+99T= NP_597681.4:n.17662+99T=
XM_011511729.1:c.43378+99T= XP_011510031.1:n.43378+99T=
XM_011511730.1:c.17272+99T= XP_011510032.1:n.17272+99T=
XM_011511731.1:c.17131+99T= XP_011510033.1:n.17131+99T=
XM_017004819.1:c.43174+99T= XP_016860308.1:n.43174+99T=
XM_017004820.1:c.38572+99T= XP_016860309.1:n.38572+99T=
XM_017004821.1:c.38569+99T= XP_016860310.1:n.38569+99T=
XM_017004822.1:c.35611+99T= XP_016860311.1:n.35611+99T=
XM_017004823.1:c.17227+99T= XP_016860312.1:n.17227+99T=
XM_024453094.1:c.38722+99T= XP_024308862.1:n.38722+99T=
XM_024453095.1:c.38719+99T= XP_024308863.1:n.38719+99T=
XM_024453096.1:c.38152+99T= XP_024308864.1:n.38152+99T=
XM_024453097.1:c.35494+99T= XP_024308865.1:n.35494+99T=
XM_024453098.1:c.35413+99T= XP_024308866.1:n.35413+99T=
XM_024453099.1:c.17176+99T= XP_024308867.1:n.17176+99T=
XM_024453100.1:c.7030+99T= XP_024308868.1:n.7030+99T=