Canonical Allele Identifier: CA2528901098
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178711133_178711134insGTC , CM000664.2:g.178711133_178711134insGTC GRCh38
NC_000002.11:g.179575860_179575861insGTC , CM000664.1:g.179575860_179575861insGTC GRCh37
NC_000002.10:g.179284105_179284106insGTC NCBI36
NG_011618.3:g.124669_124670insGAC , LRG_391:g.124669_124670insGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.24370_24371insGAC ENSP00000343764.6:p.Ala8124delinsGlyPro
ENST00000342175.11:c.13858+26948_13858+26949insGAC ENSP00000340554.6:n.13858+26948_13858+26949insGAC
ENST00000359218.10:c.13657+26948_13657+26949insGAC ENSP00000352154.5:n.13657+26948_13657+26949insGAC
ENST00000342175.10:c.13858+26948_13858+26949insGAC ENSP00000340554.6:n.13858+26948_13858+26949insGAC
ENST00000342992.10:c.24370_24371insGAC ENSP00000343764.6:p.Ala8124delinsGlyPro
ENST00000359218.9:c.13657+26948_13657+26949insGAC ENSP00000352154.5:n.13657+26948_13657+26949insGAC
ENST00000460472.6:c.13282+26948_13282+26949insGAC ENSP00000434586.1:n.13282+26948_13282+26949insGAC
ENST00000589042.5:c.28102_28103insGAC MANE Select ENSP00000467141.1:p.Ala9368delinsGlyPro
ENST00000591111.5:c.27151_27152insGAC ENSP00000465570.1:p.Ala9051delinsGlyPro
ENST00000615779.4:c.27151_27152insGAC ENSP00000483597.1:p.Ala9051delinsGlyPro
NM_001256850.1:c.27151_27152insGAC NP_001243779.1:p.Ala9051delinsGlyPro
NM_001267550.2:c.28102_28103insGAC MANE Select NP_001254479.2:p.Ala9368delinsGlyPro
NM_003319.4:c.13282+26948_13282+26949insGAC NP_003310.4:n.13282+26948_13282+26949insGAC
NM_133378.4:c.24370_24371insGAC NP_596869.4:p.Ala8124delinsGlyPro
NM_133432.3:c.13657+26948_13657+26949insGAC NP_597676.3:n.13657+26948_13657+26949insGAC
NM_133437.4:c.13858+26948_13858+26949insGAC NP_597681.4:n.13858+26948_13858+26949insGAC
XM_011511729.1:c.27199_27200insGAC XP_011510031.1:p.Ala9067delinsGlyPro
XM_011511730.1:c.13468+26948_13468+26949insGAC XP_011510032.1:n.13468+26948_13468+26949insGAC
XM_011511731.1:c.13327+26948_13327+26949insGAC XP_011510033.1:n.13327+26948_13327+26949insGAC
XM_017004819.1:c.27154_27155insGAC XP_016860308.1:p.Ala9052delinsGlyPro
XM_017004820.1:c.24373_24374insGAC XP_016860309.1:p.Ala8125delinsGlyPro
XM_017004821.1:c.24370_24371insGAC XP_016860310.1:p.Ala8124delinsGlyPro
XM_017004822.1:c.27154_27155insGAC XP_016860311.1:p.Ala9052delinsGlyPro
XM_017004823.1:c.13423+26948_13423+26949insGAC XP_016860312.1:n.13423+26948_13423+26949insGAC
XM_024453094.1:c.27154_27155insGAC XP_024308862.1:p.Ala9052delinsGlyPro
XM_024453095.1:c.27154_27155insGAC XP_024308863.1:p.Ala9052delinsGlyPro
XM_024453096.1:c.27154_27155insGAC XP_024308864.1:p.Ala9052delinsGlyPro
XM_024453097.1:c.27154_27155insGAC XP_024308865.1:p.Ala9052delinsGlyPro
XM_024453098.1:c.27154_27155insGAC XP_024308866.1:p.Ala9052delinsGlyPro
XM_024453099.1:c.13423+26948_13423+26949insGAC XP_024308867.1:n.13423+26948_13423+26949insGAC