Canonical Allele Identifier: CA349480103

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178591018A>T , CM000664.2:g.178591018A>T GRCh38
NC_000002.11:g.179455745A>T , CM000664.1:g.179455745A>T GRCh37
NC_000002.10:g.179163991A>T NCBI36
NG_011618.3:g.244785T>A , LRG_391:g.244785T>A
NG_051363.1:g.73192A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.53003T>A (TTN) ENSP00000343764.6:p.Leu17668Gln
ENST00000342175.11:c.34088T>A (TTN) ENSP00000340554.6:p.Leu11363Gln
ENST00000359218.10:c.33887T>A (TTN) ENSP00000352154.5:p.Leu11296Gln
ENST00000342175.10:c.34088T>A (TTN) ENSP00000340554.6:p.Leu11363Gln
ENST00000342992.10:c.53003T>A (TTN) ENSP00000343764.6:p.Leu17668Gln
ENST00000359218.9:c.33887T>A (TTN) ENSP00000352154.5:p.Leu11296Gln
ENST00000460472.6:c.33512T>A (TTN) ENSP00000434586.1:p.Leu11171Gln
ENST00000589042.5:c.60707T>A (TTN) MANE Select ENSP00000467141.1:p.Leu20236Gln
ENST00000591111.5:c.55784T>A (TTN) ENSP00000465570.1:p.Leu18595Gln
ENST00000615779.4:c.55784T>A (TTN) ENSP00000483597.1:p.Leu18595Gln
NM_001256850.1:c.55784T>A (TTN) NP_001243779.1:p.Leu18595Gln
NM_001267550.2:c.60707T>A (TTN) MANE Select NP_001254479.2:p.Leu20236Gln
NM_003319.4:c.33512T>A (TTN) NP_003310.4:p.Leu11171Gln
NM_133378.4:c.53003T>A (TTN) NP_596869.4:p.Leu17668Gln
NM_133432.3:c.33887T>A (TTN) NP_597676.3:p.Leu11296Gln
NM_133437.4:c.34088T>A (TTN) NP_597681.4:p.Leu11363Gln
NR_038271.1:n.597-6578A>T (TTN-AS1)
NR_038272.1:n.3189-121A>T (TTN-AS1)
XM_011511729.1:c.59804T>A (TTN) XP_011510031.1:p.Leu19935Gln
XM_011511730.1:c.33698T>A (TTN) XP_011510032.1:p.Leu11233Gln
XM_011511731.1:c.33557T>A (TTN) XP_011510033.1:p.Leu11186Gln
XM_017004819.1:c.59600T>A (TTN) XP_016860308.1:p.Leu19867Gln
XM_017004820.1:c.54998T>A (TTN) XP_016860309.1:p.Leu18333Gln
XM_017004821.1:c.54995T>A (TTN) XP_016860310.1:p.Leu18332Gln
XM_017004822.1:c.52037T>A (TTN) XP_016860311.1:p.Leu17346Gln
XM_017004823.1:c.33653T>A (TTN) XP_016860312.1:p.Leu11218Gln
XM_024453094.1:c.55148T>A (TTN) XP_024308862.1:p.Leu18383Gln
XM_024453095.1:c.55145T>A (TTN) XP_024308863.1:p.Leu18382Gln
XM_024453096.1:c.54578T>A (TTN) XP_024308864.1:p.Leu18193Gln
XM_024453097.1:c.51920T>A (TTN) XP_024308865.1:p.Leu17307Gln
XM_024453098.1:c.51839T>A (TTN) XP_024308866.1:p.Leu17280Gln
XM_024453099.1:c.33602T>A (TTN) XP_024308867.1:p.Leu11201Gln
XM_024453100.1:c.23456T>A (TTN) XP_024308868.1:p.Leu7819Gln