Canonical Allele Identifier: CA1310526707

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559634G= , CM000664.2:g.178559634G= GRCh38
NC_000002.11:g.179424361G= , CM000664.1:g.179424361G= GRCh37
NC_000002.10:g.179132607G= NCBI36
NG_011618.3:g.276169C= , LRG_391:g.276169C=
NG_051363.1:g.41808G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.78794C= (TTN) ENSP00000343764.6:p.Ala26265=
ENST00000342175.11:c.59879C= (TTN) ENSP00000340554.6:p.Ala19960=
ENST00000359218.10:c.59678C= (TTN) ENSP00000352154.5:p.Ala19893=
ENST00000342175.10:c.59879C= (TTN) ENSP00000340554.6:p.Ala19960=
ENST00000342992.10:c.78794C= (TTN) ENSP00000343764.6:p.Ala26265=
ENST00000359218.9:c.59678C= (TTN) ENSP00000352154.5:p.Ala19893=
ENST00000460472.6:c.59303C= (TTN) ENSP00000434586.1:p.Ala19768=
ENST00000589042.5:c.86498C= (TTN) MANE Select ENSP00000467141.1:p.Ala28833=
ENST00000591111.5:c.81575C= (TTN) ENSP00000465570.1:p.Ala27192=
ENST00000615779.4:c.81575C= (TTN) ENSP00000483597.1:p.Ala27192=
NM_001256850.1:c.81575C= (TTN) NP_001243779.1:p.Ala27192=
NM_001267550.2:c.86498C= (TTN) MANE Select NP_001254479.2:p.Ala28833=
NM_003319.4:c.59303C= (TTN) NP_003310.4:p.Ala19768=
NM_133378.4:c.78794C= (TTN) NP_596869.4:p.Ala26265=
NM_133432.3:c.59678C= (TTN) NP_597676.3:p.Ala19893=
NM_133437.4:c.59879C= (TTN) NP_597681.4:p.Ala19960=
NR_038271.1:n.447-11666G= (TTN-AS1)
NR_038272.1:n.2043+17273G= (TTN-AS1)
XM_011511729.1:c.85595C= (TTN) XP_011510031.1:p.Ala28532=
XM_011511730.1:c.59489C= (TTN) XP_011510032.1:p.Ala19830=
XM_011511731.1:c.59348C= (TTN) XP_011510033.1:p.Ala19783=
XM_017004819.1:c.85391C= (TTN) XP_016860308.1:p.Ala28464=
XM_017004820.1:c.80789C= (TTN) XP_016860309.1:p.Ala26930=
XM_017004821.1:c.80786C= (TTN) XP_016860310.1:p.Ala26929=
XM_017004822.1:c.77828C= (TTN) XP_016860311.1:p.Ala25943=
XM_017004823.1:c.59444C= (TTN) XP_016860312.1:p.Ala19815=
XM_024453094.1:c.80939C= (TTN) XP_024308862.1:p.Ala26980=
XM_024453095.1:c.80936C= (TTN) XP_024308863.1:p.Ala26979=
XM_024453096.1:c.80369C= (TTN) XP_024308864.1:p.Ala26790=
XM_024453097.1:c.77711C= (TTN) XP_024308865.1:p.Ala25904=
XM_024453098.1:c.77630C= (TTN) XP_024308866.1:p.Ala25877=
XM_024453099.1:c.59393C= (TTN) XP_024308867.1:p.Ala19798=
XM_024453100.1:c.49247C= (TTN) XP_024308868.1:p.Ala16416=