Canonical Allele Identifier: CA1310514682

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530489C= , CM000664.2:g.178530489C= GRCh38
NC_000002.11:g.179395216C= , CM000664.1:g.179395216C= GRCh37
NC_000002.10:g.179103462C= NCBI36
NG_011618.3:g.305314G= , LRG_391:g.305314G=
NG_051363.1:g.12663C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98422G= (TTN) ENSP00000343764.6:p.Gly32808=
ENST00000342175.11:c.79507G= (TTN) ENSP00000340554.6:p.Gly26503=
ENST00000359218.10:c.79306G= (TTN) ENSP00000352154.5:p.Gly26436=
ENST00000342175.10:c.79507G= (TTN) ENSP00000340554.6:p.Gly26503=
ENST00000342992.10:c.98422G= (TTN) ENSP00000343764.6:p.Gly32808=
ENST00000359218.9:c.79306G= (TTN) ENSP00000352154.5:p.Gly26436=
ENST00000460472.6:c.78931G= (TTN) ENSP00000434586.1:p.Gly26311=
ENST00000589042.5:c.106126G= (TTN) MANE Select ENSP00000467141.1:p.Gly35376=
ENST00000591111.5:c.101203G= (TTN) ENSP00000465570.1:p.Gly33735=
ENST00000615779.4:c.101203G= (TTN) ENSP00000483597.1:p.Gly33735=
NM_001256850.1:c.101203G= (TTN) NP_001243779.1:p.Gly33735=
NM_001267550.2:c.106126G= (TTN) MANE Select NP_001254479.2:p.Gly35376=
NM_003319.4:c.78931G= (TTN) NP_003310.4:p.Gly26311=
NM_133378.4:c.98422G= (TTN) NP_596869.4:p.Gly32808=
NM_133432.3:c.79306G= (TTN) NP_597676.3:p.Gly26436=
NM_133437.4:c.79507G= (TTN) NP_597681.4:p.Gly26503=
NR_038271.1:n.446+6853C= (TTN-AS1)
NR_038272.1:n.220-5243C= (TTN-AS1)
XM_011511729.1:c.105223G= (TTN) XP_011510031.1:p.Gly35075=
XM_011511730.1:c.79117G= (TTN) XP_011510032.1:p.Gly26373=
XM_011511731.1:c.78976G= (TTN) XP_011510033.1:p.Gly26326=
XM_017004819.1:c.105019G= (TTN) XP_016860308.1:p.Gly35007=
XM_017004820.1:c.100417G= (TTN) XP_016860309.1:p.Gly33473=
XM_017004821.1:c.100414G= (TTN) XP_016860310.1:p.Gly33472=
XM_017004822.1:c.97456G= (TTN) XP_016860311.1:p.Gly32486=
XM_017004823.1:c.79072G= (TTN) XP_016860312.1:p.Gly26358=
XM_024453094.1:c.100567G= (TTN) XP_024308862.1:p.Gly33523=
XM_024453095.1:c.100564G= (TTN) XP_024308863.1:p.Gly33522=
XM_024453096.1:c.99997G= (TTN) XP_024308864.1:p.Gly33333=
XM_024453097.1:c.97339G= (TTN) XP_024308865.1:p.Gly32447=
XM_024453098.1:c.97258G= (TTN) XP_024308866.1:p.Gly32420=
XM_024453099.1:c.79021G= (TTN) XP_024308867.1:p.Gly26341=
XM_024453100.1:c.68875G= (TTN) XP_024308868.1:p.Gly22959=