Canonical Allele Identifier: CA1310537030

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178584477T= , CM000664.2:g.178584477T= GRCh38
NC_000002.11:g.179449204T= , CM000664.1:g.179449204T= GRCh37
NC_000002.10:g.179157450T= NCBI36
NG_011618.3:g.251326A= , LRG_391:g.251326A=
NG_051363.1:g.66651T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.57370A= (TTN) ENSP00000343764.6:p.Ile19124=
ENST00000342175.11:c.38455A= (TTN) ENSP00000340554.6:p.Ile12819=
ENST00000359218.10:c.38254A= (TTN) ENSP00000352154.5:p.Ile12752=
ENST00000342175.10:c.38455A= (TTN) ENSP00000340554.6:p.Ile12819=
ENST00000342992.10:c.57370A= (TTN) ENSP00000343764.6:p.Ile19124=
ENST00000359218.9:c.38254A= (TTN) ENSP00000352154.5:p.Ile12752=
ENST00000460472.6:c.37879A= (TTN) ENSP00000434586.1:p.Ile12627=
ENST00000589042.5:c.65074A= (TTN) MANE Select ENSP00000467141.1:p.Ile21692=
ENST00000591111.5:c.60151A= (TTN) ENSP00000465570.1:p.Ile20051=
ENST00000615779.4:c.60151A= (TTN) ENSP00000483597.1:p.Ile20051=
NM_001256850.1:c.60151A= (TTN) NP_001243779.1:p.Ile20051=
NM_001267550.2:c.65074A= (TTN) MANE Select NP_001254479.2:p.Ile21692=
NM_003319.4:c.37879A= (TTN) NP_003310.4:p.Ile12627=
NM_133378.4:c.57370A= (TTN) NP_596869.4:p.Ile19124=
NM_133432.3:c.38254A= (TTN) NP_597676.3:p.Ile12752=
NM_133437.4:c.38455A= (TTN) NP_597681.4:p.Ile12819=
NR_038271.1:n.596+13028T= (TTN-AS1)
NR_038272.1:n.2768-96T= (TTN-AS1)
XM_011511729.1:c.64171A= (TTN) XP_011510031.1:p.Ile21391=
XM_011511730.1:c.38065A= (TTN) XP_011510032.1:p.Ile12689=
XM_011511731.1:c.37924A= (TTN) XP_011510033.1:p.Ile12642=
XM_017004819.1:c.63967A= (TTN) XP_016860308.1:p.Ile21323=
XM_017004820.1:c.59365A= (TTN) XP_016860309.1:p.Ile19789=
XM_017004821.1:c.59362A= (TTN) XP_016860310.1:p.Ile19788=
XM_017004822.1:c.56404A= (TTN) XP_016860311.1:p.Ile18802=
XM_017004823.1:c.38020A= (TTN) XP_016860312.1:p.Ile12674=
XM_024453094.1:c.59515A= (TTN) XP_024308862.1:p.Ile19839=
XM_024453095.1:c.59512A= (TTN) XP_024308863.1:p.Ile19838=
XM_024453096.1:c.58945A= (TTN) XP_024308864.1:p.Ile19649=
XM_024453097.1:c.56287A= (TTN) XP_024308865.1:p.Ile18763=
XM_024453098.1:c.56206A= (TTN) XP_024308866.1:p.Ile18736=
XM_024453099.1:c.37969A= (TTN) XP_024308867.1:p.Ile12657=
XM_024453100.1:c.27823A= (TTN) XP_024308868.1:p.Ile9275=