Canonical Allele Identifier: CA1310514744

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530555G= , CM000664.2:g.178530555G= GRCh38
NC_000002.11:g.179395282G= , CM000664.1:g.179395282G= GRCh37
NC_000002.10:g.179103528G= NCBI36
NG_011618.3:g.305248C= , LRG_391:g.305248C=
NG_051363.1:g.12729G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98356C= (TTN) ENSP00000343764.6:p.Gln32786=
ENST00000342175.11:c.79441C= (TTN) ENSP00000340554.6:p.Gln26481=
ENST00000359218.10:c.79240C= (TTN) ENSP00000352154.5:p.Gln26414=
ENST00000342175.10:c.79441C= (TTN) ENSP00000340554.6:p.Gln26481=
ENST00000342992.10:c.98356C= (TTN) ENSP00000343764.6:p.Gln32786=
ENST00000359218.9:c.79240C= (TTN) ENSP00000352154.5:p.Gln26414=
ENST00000460472.6:c.78865C= (TTN) ENSP00000434586.1:p.Gln26289=
ENST00000589042.5:c.106060C= (TTN) MANE Select ENSP00000467141.1:p.Gln35354=
ENST00000591111.5:c.101137C= (TTN) ENSP00000465570.1:p.Gln33713=
ENST00000615779.4:c.101137C= (TTN) ENSP00000483597.1:p.Gln33713=
NM_001256850.1:c.101137C= (TTN) NP_001243779.1:p.Gln33713=
NM_001267550.2:c.106060C= (TTN) MANE Select NP_001254479.2:p.Gln35354=
NM_003319.4:c.78865C= (TTN) NP_003310.4:p.Gln26289=
NM_133378.4:c.98356C= (TTN) NP_596869.4:p.Gln32786=
NM_133432.3:c.79240C= (TTN) NP_597676.3:p.Gln26414=
NM_133437.4:c.79441C= (TTN) NP_597681.4:p.Gln26481=
NR_038271.1:n.446+6919G= (TTN-AS1)
NR_038272.1:n.220-5177G= (TTN-AS1)
XM_011511729.1:c.105157C= (TTN) XP_011510031.1:p.Gln35053=
XM_011511730.1:c.79051C= (TTN) XP_011510032.1:p.Gln26351=
XM_011511731.1:c.78910C= (TTN) XP_011510033.1:p.Gln26304=
XM_017004819.1:c.104953C= (TTN) XP_016860308.1:p.Gln34985=
XM_017004820.1:c.100351C= (TTN) XP_016860309.1:p.Gln33451=
XM_017004821.1:c.100348C= (TTN) XP_016860310.1:p.Gln33450=
XM_017004822.1:c.97390C= (TTN) XP_016860311.1:p.Gln32464=
XM_017004823.1:c.79006C= (TTN) XP_016860312.1:p.Gln26336=
XM_024453094.1:c.100501C= (TTN) XP_024308862.1:p.Gln33501=
XM_024453095.1:c.100498C= (TTN) XP_024308863.1:p.Gln33500=
XM_024453096.1:c.99931C= (TTN) XP_024308864.1:p.Gln33311=
XM_024453097.1:c.97273C= (TTN) XP_024308865.1:p.Gln32425=
XM_024453098.1:c.97192C= (TTN) XP_024308866.1:p.Gln32398=
XM_024453099.1:c.78955C= (TTN) XP_024308867.1:p.Gln26319=
XM_024453100.1:c.68809C= (TTN) XP_024308868.1:p.Gln22937=