Canonical Allele Identifier: CA1310550894

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618058C= , CM000664.2:g.178618058C= GRCh38
NC_000002.11:g.179482785C= , CM000664.1:g.179482785C= GRCh37
NC_000002.10:g.179191030C= NCBI36
NG_011618.3:g.217745G= , LRG_391:g.217745G=
NG_051363.1:g.100232C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.39589G= (TTN) ENSP00000343764.6:p.Val13197=
ENST00000342175.11:c.20674G= (TTN) ENSP00000340554.6:p.Val6892=
ENST00000359218.10:c.20473G= (TTN) ENSP00000352154.5:p.Val6825=
ENST00000342175.10:c.20674G= (TTN) ENSP00000340554.6:p.Val6892=
ENST00000342992.10:c.39589G= (TTN) ENSP00000343764.6:p.Val13197=
ENST00000359218.9:c.20473G= (TTN) ENSP00000352154.5:p.Val6825=
ENST00000460472.6:c.20098G= (TTN) ENSP00000434586.1:p.Val6700=
ENST00000589042.5:c.47293G= (TTN) MANE Select ENSP00000467141.1:p.Val15765=
ENST00000591111.5:c.42370G= (TTN) ENSP00000465570.1:p.Val14124=
ENST00000615779.4:c.42370G= (TTN) ENSP00000483597.1:p.Val14124=
NM_001256850.1:c.42370G= (TTN) NP_001243779.1:p.Val14124=
NM_001267550.2:c.47293G= (TTN) MANE Select NP_001254479.2:p.Val15765=
NM_003319.4:c.20098G= (TTN) NP_003310.4:p.Val6700=
NM_133378.4:c.39589G= (TTN) NP_596869.4:p.Val13197=
NM_133432.3:c.20473G= (TTN) NP_597676.3:p.Val6825=
NM_133437.4:c.20674G= (TTN) NP_597681.4:p.Val6892=
NR_038271.1:n.1605-1695C= (TTN-AS1)
XM_011511729.1:c.46390G= (TTN) XP_011510031.1:p.Val15464=
XM_011511730.1:c.20284G= (TTN) XP_011510032.1:p.Val6762=
XM_011511731.1:c.20143G= (TTN) XP_011510033.1:p.Val6715=
XM_017004819.1:c.46186G= (TTN) XP_016860308.1:p.Val15396=
XM_017004820.1:c.41584G= (TTN) XP_016860309.1:p.Val13862=
XM_017004821.1:c.41581G= (TTN) XP_016860310.1:p.Val13861=
XM_017004822.1:c.38623G= (TTN) XP_016860311.1:p.Val12875=
XM_017004823.1:c.20239G= (TTN) XP_016860312.1:p.Val6747=
XM_024453094.1:c.41734G= (TTN) XP_024308862.1:p.Val13912=
XM_024453095.1:c.41731G= (TTN) XP_024308863.1:p.Val13911=
XM_024453096.1:c.41164G= (TTN) XP_024308864.1:p.Val13722=
XM_024453097.1:c.38506G= (TTN) XP_024308865.1:p.Val12836=
XM_024453098.1:c.38425G= (TTN) XP_024308866.1:p.Val12809=
XM_024453099.1:c.20188G= (TTN) XP_024308867.1:p.Val6730=
XM_024453100.1:c.10042G= (TTN) XP_024308868.1:p.Val3348=