Canonical Allele Identifier: CA2586970733

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530283_178530284dup , CM000664.2:g.178530283_178530284dup GRCh38
NC_000002.11:g.179395010_179395011dup , CM000664.1:g.179395010_179395011dup GRCh37
NC_000002.10:g.179103256_179103257dup NCBI36
NG_011618.3:g.305519_305520dup , LRG_391:g.305519_305520dup
NG_051363.1:g.12457_12458dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98627_98628dup (TTN) ENSP00000343764.6:p.Gly32877LeufsTer?
ENST00000342175.11:c.79712_79713dup (TTN) ENSP00000340554.6:p.Gly26572LeufsTer?
ENST00000359218.10:c.79511_79512dup (TTN) ENSP00000352154.5:p.Gly26505LeufsTer?
ENST00000342175.10:c.79712_79713dup (TTN) ENSP00000340554.6:p.Gly26572LeufsTer?
ENST00000342992.10:c.98627_98628dup (TTN) ENSP00000343764.6:p.Gly32877LeufsTer?
ENST00000359218.9:c.79511_79512dup (TTN) ENSP00000352154.5:p.Gly26505LeufsTer?
ENST00000460472.6:c.79136_79137dup (TTN) ENSP00000434586.1:p.Gly26380LeufsTer?
ENST00000589042.5:c.106331_106332dup (TTN) MANE Select ENSP00000467141.1:p.Gly35445LeufsTer?
ENST00000591111.5:c.101408_101409dup (TTN) ENSP00000465570.1:p.Gly33804LeufsTer?
ENST00000615779.4:c.101408_101409dup (TTN) ENSP00000483597.1:p.Gly33804LeufsTer?
NM_001256850.1:c.101408_101409dup (TTN) NP_001243779.1:p.Gly33804LeufsTer?
NM_001267550.2:c.106331_106332dup (TTN) MANE Select NP_001254479.2:p.Gly35445LeufsTer?
NM_003319.4:c.79136_79137dup (TTN) NP_003310.4:p.Gly26380LeufsTer?
NM_133378.4:c.98627_98628dup (TTN) NP_596869.4:p.Gly32877LeufsTer?
NM_133432.3:c.79511_79512dup (TTN) NP_597676.3:p.Gly26505LeufsTer?
NM_133437.4:c.79712_79713dup (TTN) NP_597681.4:p.Gly26572LeufsTer?
NR_038271.1:n.446+6647_446+6648dup (TTN-AS1)
NR_038272.1:n.220-5449_220-5448dup (TTN-AS1)
XM_011511729.1:c.105428_105429dup (TTN) XP_011510031.1:p.Gly35144LeufsTer?
XM_011511730.1:c.79322_79323dup (TTN) XP_011510032.1:p.Gly26442LeufsTer?
XM_011511731.1:c.79181_79182dup (TTN) XP_011510033.1:p.Gly26395LeufsTer?
XM_017004819.1:c.105224_105225dup (TTN) XP_016860308.1:p.Gly35076LeufsTer?
XM_017004820.1:c.100622_100623dup (TTN) XP_016860309.1:p.Gly33542LeufsTer?
XM_017004821.1:c.100619_100620dup (TTN) XP_016860310.1:p.Gly33541LeufsTer?
XM_017004822.1:c.97661_97662dup (TTN) XP_016860311.1:p.Gly32555LeufsTer?
XM_017004823.1:c.79277_79278dup (TTN) XP_016860312.1:p.Gly26427LeufsTer?
XM_024453094.1:c.100772_100773dup (TTN) XP_024308862.1:p.Gly33592LeufsTer?
XM_024453095.1:c.100769_100770dup (TTN) XP_024308863.1:p.Gly33591LeufsTer?
XM_024453096.1:c.100202_100203dup (TTN) XP_024308864.1:p.Gly33402LeufsTer?
XM_024453097.1:c.97544_97545dup (TTN) XP_024308865.1:p.Gly32516LeufsTer?
XM_024453098.1:c.97463_97464dup (TTN) XP_024308866.1:p.Gly32489LeufsTer?
XM_024453099.1:c.79226_79227dup (TTN) XP_024308867.1:p.Gly26410LeufsTer?
XM_024453100.1:c.69080_69081dup (TTN) XP_024308868.1:p.Gly23028LeufsTer?