Canonical Allele Identifier: CA1310516560

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178539970_178539971delinsGA , CM000664.2:g.178539970_178539971delinsGA GRCh38
NC_000002.11:g.179404697_179404698delinsGA , CM000664.1:g.179404697_179404698delinsGA GRCh37
NC_000002.10:g.179112943_179112944delinsGA NCBI36
NG_011618.3:g.295832_295833delinsTC , LRG_391:g.295832_295833delinsTC
NG_051363.1:g.22144_22145delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.90395-5_90395-4delinsTC (TTN) ENSP00000343764.6:n.90395-5_90395-4delins...
ENST00000342175.11:c.71480-5_71480-4delinsTC (TTN) ENSP00000340554.6:n.71480-5_71480-4delins...
ENST00000359218.10:c.71279-5_71279-4delinsTC (TTN) ENSP00000352154.5:n.71279-5_71279-4delins...
ENST00000342175.10:c.71480-5_71480-4delinsTC (TTN) ENSP00000340554.6:n.71480-5_71480-4delins...
ENST00000342992.10:c.90395-5_90395-4delinsTC (TTN) ENSP00000343764.6:n.90395-5_90395-4delins...
ENST00000359218.9:c.71279-5_71279-4delinsTC (TTN) ENSP00000352154.5:n.71279-5_71279-4delins...
ENST00000460472.6:c.70904-5_70904-4delinsTC (TTN) ENSP00000434586.1:n.70904-5_70904-4delins...
ENST00000589042.5:c.98099-5_98099-4delinsTC (TTN) MANE Select ENSP00000467141.1:n.98099-5_98099-4delins...
ENST00000591111.5:c.93176-5_93176-4delinsTC (TTN) ENSP00000465570.1:n.93176-5_93176-4delins...
ENST00000615779.4:c.93176-5_93176-4delinsTC (TTN) ENSP00000483597.1:n.93176-5_93176-4delins...
NM_001256850.1:c.93176-5_93176-4delinsTC (TTN) NP_001243779.1:n.93176-5_93176-4delinsTC
NM_001267550.2:c.98099-5_98099-4delinsTC (TTN) MANE Select NP_001254479.2:n.98099-5_98099-4delinsTC
NM_003319.4:c.70904-5_70904-4delinsTC (TTN) NP_003310.4:n.70904-5_70904-4delinsTC
NM_133378.4:c.90395-5_90395-4delinsTC (TTN) NP_596869.4:n.90395-5_90395-4delinsTC
NM_133432.3:c.71279-5_71279-4delinsTC (TTN) NP_597676.3:n.71279-5_71279-4delinsTC
NM_133437.4:c.71480-5_71480-4delinsTC (TTN) NP_597681.4:n.71480-5_71480-4delinsTC
NR_038271.1:n.446+16334_446+16335delinsGA (TTN-AS1)
NR_038272.1:n.1840+80_1840+81delinsGA (TTN-AS1)
XM_011511729.1:c.97196-5_97196-4delinsTC (TTN) XP_011510031.1:n.97196-5_97196-4delinsTC
XM_011511730.1:c.71090-5_71090-4delinsTC (TTN) XP_011510032.1:n.71090-5_71090-4delinsTC
XM_011511731.1:c.70949-5_70949-4delinsTC (TTN) XP_011510033.1:n.70949-5_70949-4delinsTC
XM_017004819.1:c.96992-5_96992-4delinsTC (TTN) XP_016860308.1:n.96992-5_96992-4delinsTC
XM_017004820.1:c.92390-5_92390-4delinsTC (TTN) XP_016860309.1:n.92390-5_92390-4delinsTC
XM_017004821.1:c.92387-5_92387-4delinsTC (TTN) XP_016860310.1:n.92387-5_92387-4delinsTC
XM_017004822.1:c.89429-5_89429-4delinsTC (TTN) XP_016860311.1:n.89429-5_89429-4delinsTC
XM_017004823.1:c.71045-5_71045-4delinsTC (TTN) XP_016860312.1:n.71045-5_71045-4delinsTC
XM_024453094.1:c.92540-5_92540-4delinsTC (TTN) XP_024308862.1:n.92540-5_92540-4delinsTC
XM_024453095.1:c.92537-5_92537-4delinsTC (TTN) XP_024308863.1:n.92537-5_92537-4delinsTC
XM_024453096.1:c.91970-5_91970-4delinsTC (TTN) XP_024308864.1:n.91970-5_91970-4delinsTC
XM_024453097.1:c.89312-5_89312-4delinsTC (TTN) XP_024308865.1:n.89312-5_89312-4delinsTC
XM_024453098.1:c.89231-5_89231-4delinsTC (TTN) XP_024308866.1:n.89231-5_89231-4delinsTC
XM_024453099.1:c.70994-5_70994-4delinsTC (TTN) XP_024308867.1:n.70994-5_70994-4delinsTC
XM_024453100.1:c.60848-5_60848-4delinsTC (TTN) XP_024308868.1:n.60848-5_60848-4delinsTC