Canonical Allele Identifier: CA1310520099

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178549776C= , CM000664.2:g.178549776C= GRCh38
NC_000002.11:g.179414503C= , CM000664.1:g.179414503C= GRCh37
NC_000002.10:g.179122749C= NCBI36
NG_011618.3:g.286027G= , LRG_391:g.286027G=
NG_051363.1:g.31950C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.84242G= (TTN) ENSP00000343764.6:p.Cys28081=
ENST00000342175.11:c.65327G= (TTN) ENSP00000340554.6:p.Cys21776=
ENST00000359218.10:c.65126G= (TTN) ENSP00000352154.5:p.Cys21709=
ENST00000342175.10:c.65327G= (TTN) ENSP00000340554.6:p.Cys21776=
ENST00000342992.10:c.84242G= (TTN) ENSP00000343764.6:p.Cys28081=
ENST00000359218.9:c.65126G= (TTN) ENSP00000352154.5:p.Cys21709=
ENST00000460472.6:c.64751G= (TTN) ENSP00000434586.1:p.Cys21584=
ENST00000589042.5:c.91946G= (TTN) MANE Select ENSP00000467141.1:p.Cys30649=
ENST00000591111.5:c.87023G= (TTN) ENSP00000465570.1:p.Cys29008=
ENST00000615779.4:c.87023G= (TTN) ENSP00000483597.1:p.Cys29008=
NM_001256850.1:c.87023G= (TTN) NP_001243779.1:p.Cys29008=
NM_001267550.2:c.91946G= (TTN) MANE Select NP_001254479.2:p.Cys30649=
NM_003319.4:c.64751G= (TTN) NP_003310.4:p.Cys21584=
NM_133378.4:c.84242G= (TTN) NP_596869.4:p.Cys28081=
NM_133432.3:c.65126G= (TTN) NP_597676.3:p.Cys21709=
NM_133437.4:c.65327G= (TTN) NP_597681.4:p.Cys21776=
NR_038271.1:n.447-21524C= (TTN-AS1)
NR_038272.1:n.2043+7415C= (TTN-AS1)
XM_011511729.1:c.91043G= (TTN) XP_011510031.1:p.Cys30348=
XM_011511730.1:c.64937G= (TTN) XP_011510032.1:p.Cys21646=
XM_011511731.1:c.64796G= (TTN) XP_011510033.1:p.Cys21599=
XM_017004819.1:c.90839G= (TTN) XP_016860308.1:p.Cys30280=
XM_017004820.1:c.86237G= (TTN) XP_016860309.1:p.Cys28746=
XM_017004821.1:c.86234G= (TTN) XP_016860310.1:p.Cys28745=
XM_017004822.1:c.83276G= (TTN) XP_016860311.1:p.Cys27759=
XM_017004823.1:c.64892G= (TTN) XP_016860312.1:p.Cys21631=
XM_024453094.1:c.86387G= (TTN) XP_024308862.1:p.Cys28796=
XM_024453095.1:c.86384G= (TTN) XP_024308863.1:p.Cys28795=
XM_024453096.1:c.85817G= (TTN) XP_024308864.1:p.Cys28606=
XM_024453097.1:c.83159G= (TTN) XP_024308865.1:p.Cys27720=
XM_024453098.1:c.83078G= (TTN) XP_024308866.1:p.Cys27693=
XM_024453099.1:c.64841G= (TTN) XP_024308867.1:p.Cys21614=
XM_024453100.1:c.54695G= (TTN) XP_024308868.1:p.Cys18232=