Canonical Allele Identifier: CA1310532245

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178573878G= , CM000664.2:g.178573878G= GRCh38
NC_000002.11:g.179438605G= , CM000664.1:g.179438605G= GRCh37
NC_000002.10:g.179146851G= NCBI36
NG_011618.3:g.261925C= , LRG_391:g.261925C=
NG_051363.1:g.56052G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.64550C= (TTN) ENSP00000343764.6:p.Thr21517=
ENST00000342175.11:c.45635C= (TTN) ENSP00000340554.6:p.Thr15212=
ENST00000359218.10:c.45434C= (TTN) ENSP00000352154.5:p.Thr15145=
ENST00000342175.10:c.45635C= (TTN) ENSP00000340554.6:p.Thr15212=
ENST00000342992.10:c.64550C= (TTN) ENSP00000343764.6:p.Thr21517=
ENST00000359218.9:c.45434C= (TTN) ENSP00000352154.5:p.Thr15145=
ENST00000460472.6:c.45059C= (TTN) ENSP00000434586.1:p.Thr15020=
ENST00000589042.5:c.72254C= (TTN) MANE Select ENSP00000467141.1:p.Thr24085=
ENST00000591111.5:c.67331C= (TTN) ENSP00000465570.1:p.Thr22444=
ENST00000615779.4:c.67331C= (TTN) ENSP00000483597.1:p.Thr22444=
NM_001256850.1:c.67331C= (TTN) NP_001243779.1:p.Thr22444=
NM_001267550.2:c.72254C= (TTN) MANE Select NP_001254479.2:p.Thr24085=
NM_003319.4:c.45059C= (TTN) NP_003310.4:p.Thr15020=
NM_133378.4:c.64550C= (TTN) NP_596869.4:p.Thr21517=
NM_133432.3:c.45434C= (TTN) NP_597676.3:p.Thr15145=
NM_133437.4:c.45635C= (TTN) NP_597681.4:p.Thr15212=
NR_038271.1:n.596+2429G= (TTN-AS1)
NR_038272.1:n.2044-8694G= (TTN-AS1)
XM_011511729.1:c.71351C= (TTN) XP_011510031.1:p.Thr23784=
XM_011511730.1:c.45245C= (TTN) XP_011510032.1:p.Thr15082=
XM_011511731.1:c.45104C= (TTN) XP_011510033.1:p.Thr15035=
XM_017004819.1:c.71147C= (TTN) XP_016860308.1:p.Thr23716=
XM_017004820.1:c.66545C= (TTN) XP_016860309.1:p.Thr22182=
XM_017004821.1:c.66542C= (TTN) XP_016860310.1:p.Thr22181=
XM_017004822.1:c.63584C= (TTN) XP_016860311.1:p.Thr21195=
XM_017004823.1:c.45200C= (TTN) XP_016860312.1:p.Thr15067=
XM_024453094.1:c.66695C= (TTN) XP_024308862.1:p.Thr22232=
XM_024453095.1:c.66692C= (TTN) XP_024308863.1:p.Thr22231=
XM_024453096.1:c.66125C= (TTN) XP_024308864.1:p.Thr22042=
XM_024453097.1:c.63467C= (TTN) XP_024308865.1:p.Thr21156=
XM_024453098.1:c.63386C= (TTN) XP_024308866.1:p.Thr21129=
XM_024453099.1:c.45149C= (TTN) XP_024308867.1:p.Thr15050=
XM_024453100.1:c.35003C= (TTN) XP_024308868.1:p.Thr11668=