Canonical Allele Identifier: CA1310529442

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178566265C= , CM000664.2:g.178566265C= GRCh38
NC_000002.11:g.179430992C= , CM000664.1:g.179430992C= GRCh37
NC_000002.10:g.179139238C= NCBI36
NG_011618.3:g.269538G= , LRG_391:g.269538G=
NG_051363.1:g.48439C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.72163G= (TTN) ENSP00000343764.6:p.Glu24055=
ENST00000342175.11:c.53248G= (TTN) ENSP00000340554.6:p.Glu17750=
ENST00000359218.10:c.53047G= (TTN) ENSP00000352154.5:p.Glu17683=
ENST00000342175.10:c.53248G= (TTN) ENSP00000340554.6:p.Glu17750=
ENST00000342992.10:c.72163G= (TTN) ENSP00000343764.6:p.Glu24055=
ENST00000359218.9:c.53047G= (TTN) ENSP00000352154.5:p.Glu17683=
ENST00000460472.6:c.52672G= (TTN) ENSP00000434586.1:p.Glu17558=
ENST00000589042.5:c.79867G= (TTN) MANE Select ENSP00000467141.1:p.Glu26623=
ENST00000591111.5:c.74944G= (TTN) ENSP00000465570.1:p.Glu24982=
ENST00000615779.4:c.74944G= (TTN) ENSP00000483597.1:p.Glu24982=
NM_001256850.1:c.74944G= (TTN) NP_001243779.1:p.Glu24982=
NM_001267550.2:c.79867G= (TTN) MANE Select NP_001254479.2:p.Glu26623=
NM_003319.4:c.52672G= (TTN) NP_003310.4:p.Glu17558=
NM_133378.4:c.72163G= (TTN) NP_596869.4:p.Glu24055=
NM_133432.3:c.53047G= (TTN) NP_597676.3:p.Glu17683=
NM_133437.4:c.53248G= (TTN) NP_597681.4:p.Glu17750=
NR_038271.1:n.447-5035C= (TTN-AS1)
NR_038272.1:n.2044-16307C= (TTN-AS1)
XM_011511729.1:c.78964G= (TTN) XP_011510031.1:p.Glu26322=
XM_011511730.1:c.52858G= (TTN) XP_011510032.1:p.Glu17620=
XM_011511731.1:c.52717G= (TTN) XP_011510033.1:p.Glu17573=
XM_017004819.1:c.78760G= (TTN) XP_016860308.1:p.Glu26254=
XM_017004820.1:c.74158G= (TTN) XP_016860309.1:p.Glu24720=
XM_017004821.1:c.74155G= (TTN) XP_016860310.1:p.Glu24719=
XM_017004822.1:c.71197G= (TTN) XP_016860311.1:p.Glu23733=
XM_017004823.1:c.52813G= (TTN) XP_016860312.1:p.Glu17605=
XM_024453094.1:c.74308G= (TTN) XP_024308862.1:p.Glu24770=
XM_024453095.1:c.74305G= (TTN) XP_024308863.1:p.Glu24769=
XM_024453096.1:c.73738G= (TTN) XP_024308864.1:p.Glu24580=
XM_024453097.1:c.71080G= (TTN) XP_024308865.1:p.Glu23694=
XM_024453098.1:c.70999G= (TTN) XP_024308866.1:p.Glu23667=
XM_024453099.1:c.52762G= (TTN) XP_024308867.1:p.Glu17588=
XM_024453100.1:c.42616G= (TTN) XP_024308868.1:p.Glu14206=