Canonical Allele Identifier: CA1310511654

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530245C= , CM000664.2:g.178530245C= GRCh38
NC_000002.11:g.179394972C= , CM000664.1:g.179394972C= GRCh37
NC_000002.10:g.179103218C= NCBI36
NG_011618.3:g.305558G= , LRG_391:g.305558G=
NG_051363.1:g.12419C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98666G= (TTN) ENSP00000343764.6:p.Gly32889=
ENST00000342175.11:c.79751G= (TTN) ENSP00000340554.6:p.Gly26584=
ENST00000359218.10:c.79550G= (TTN) ENSP00000352154.5:p.Gly26517=
ENST00000342175.10:c.79751G= (TTN) ENSP00000340554.6:p.Gly26584=
ENST00000342992.10:c.98666G= (TTN) ENSP00000343764.6:p.Gly32889=
ENST00000359218.9:c.79550G= (TTN) ENSP00000352154.5:p.Gly26517=
ENST00000460472.6:c.79175G= (TTN) ENSP00000434586.1:p.Gly26392=
ENST00000589042.5:c.106370G= (TTN) MANE Select ENSP00000467141.1:p.Gly35457=
ENST00000591111.5:c.101447G= (TTN) ENSP00000465570.1:p.Gly33816=
ENST00000615779.4:c.101447G= (TTN) ENSP00000483597.1:p.Gly33816=
NM_001256850.1:c.101447G= (TTN) NP_001243779.1:p.Gly33816=
NM_001267550.2:c.106370G= (TTN) MANE Select NP_001254479.2:p.Gly35457=
NM_003319.4:c.79175G= (TTN) NP_003310.4:p.Gly26392=
NM_133378.4:c.98666G= (TTN) NP_596869.4:p.Gly32889=
NM_133432.3:c.79550G= (TTN) NP_597676.3:p.Gly26517=
NM_133437.4:c.79751G= (TTN) NP_597681.4:p.Gly26584=
NR_038271.1:n.446+6609C= (TTN-AS1)
NR_038272.1:n.220-5487C= (TTN-AS1)
XM_011511729.1:c.105467G= (TTN) XP_011510031.1:p.Gly35156=
XM_011511730.1:c.79361G= (TTN) XP_011510032.1:p.Gly26454=
XM_011511731.1:c.79220G= (TTN) XP_011510033.1:p.Gly26407=
XM_017004819.1:c.105263G= (TTN) XP_016860308.1:p.Gly35088=
XM_017004820.1:c.100661G= (TTN) XP_016860309.1:p.Gly33554=
XM_017004821.1:c.100658G= (TTN) XP_016860310.1:p.Gly33553=
XM_017004822.1:c.97700G= (TTN) XP_016860311.1:p.Gly32567=
XM_017004823.1:c.79316G= (TTN) XP_016860312.1:p.Gly26439=
XM_024453094.1:c.100811G= (TTN) XP_024308862.1:p.Gly33604=
XM_024453095.1:c.100808G= (TTN) XP_024308863.1:p.Gly33603=
XM_024453096.1:c.100241G= (TTN) XP_024308864.1:p.Gly33414=
XM_024453097.1:c.97583G= (TTN) XP_024308865.1:p.Gly32528=
XM_024453098.1:c.97502G= (TTN) XP_024308866.1:p.Gly32501=
XM_024453099.1:c.79265G= (TTN) XP_024308867.1:p.Gly26422=
XM_024453100.1:c.69119G= (TTN) XP_024308868.1:p.Gly23040=