Canonical Allele Identifier: CA1310539406

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178589315T= , CM000664.2:g.178589315T= GRCh38
NC_000002.11:g.179454042T= , CM000664.1:g.179454042T= GRCh37
NC_000002.10:g.179162288T= NCBI36
NG_011618.3:g.246488A= , LRG_391:g.246488A=
NG_051363.1:g.71489T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.54706A= (TTN) ENSP00000343764.6:p.Thr18236=
ENST00000342175.11:c.35791A= (TTN) ENSP00000340554.6:p.Thr11931=
ENST00000359218.10:c.35590A= (TTN) ENSP00000352154.5:p.Thr11864=
ENST00000342175.10:c.35791A= (TTN) ENSP00000340554.6:p.Thr11931=
ENST00000342992.10:c.54706A= (TTN) ENSP00000343764.6:p.Thr18236=
ENST00000359218.9:c.35590A= (TTN) ENSP00000352154.5:p.Thr11864=
ENST00000460472.6:c.35215A= (TTN) ENSP00000434586.1:p.Thr11739=
ENST00000589042.5:c.62410A= (TTN) MANE Select ENSP00000467141.1:p.Thr20804=
ENST00000591111.5:c.57487A= (TTN) ENSP00000465570.1:p.Thr19163=
ENST00000615779.4:c.57487A= (TTN) ENSP00000483597.1:p.Thr19163=
NM_001256850.1:c.57487A= (TTN) NP_001243779.1:p.Thr19163=
NM_001267550.2:c.62410A= (TTN) MANE Select NP_001254479.2:p.Thr20804=
NM_003319.4:c.35215A= (TTN) NP_003310.4:p.Thr11739=
NM_133378.4:c.54706A= (TTN) NP_596869.4:p.Thr18236=
NM_133432.3:c.35590A= (TTN) NP_597676.3:p.Thr11864=
NM_133437.4:c.35791A= (TTN) NP_597681.4:p.Thr11931=
NR_038271.1:n.597-8281T= (TTN-AS1)
NR_038272.1:n.3189-1824T= (TTN-AS1)
XM_011511729.1:c.61507A= (TTN) XP_011510031.1:p.Thr20503=
XM_011511730.1:c.35401A= (TTN) XP_011510032.1:p.Thr11801=
XM_011511731.1:c.35260A= (TTN) XP_011510033.1:p.Thr11754=
XM_017004819.1:c.61303A= (TTN) XP_016860308.1:p.Thr20435=
XM_017004820.1:c.56701A= (TTN) XP_016860309.1:p.Thr18901=
XM_017004821.1:c.56698A= (TTN) XP_016860310.1:p.Thr18900=
XM_017004822.1:c.53740A= (TTN) XP_016860311.1:p.Thr17914=
XM_017004823.1:c.35356A= (TTN) XP_016860312.1:p.Thr11786=
XM_024453094.1:c.56851A= (TTN) XP_024308862.1:p.Thr18951=
XM_024453095.1:c.56848A= (TTN) XP_024308863.1:p.Thr18950=
XM_024453096.1:c.56281A= (TTN) XP_024308864.1:p.Thr18761=
XM_024453097.1:c.53623A= (TTN) XP_024308865.1:p.Thr17875=
XM_024453098.1:c.53542A= (TTN) XP_024308866.1:p.Thr17848=
XM_024453099.1:c.35305A= (TTN) XP_024308867.1:p.Thr11769=
XM_024453100.1:c.25159A= (TTN) XP_024308868.1:p.Thr8387=