Canonical Allele Identifier: CA1310526715

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559649T= , CM000664.2:g.178559649T= GRCh38
NC_000002.11:g.179424376T= , CM000664.1:g.179424376T= GRCh37
NC_000002.10:g.179132622T= NCBI36
NG_011618.3:g.276154A= , LRG_391:g.276154A=
NG_051363.1:g.41823T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.78779A= (TTN) ENSP00000343764.6:p.Gln26260=
ENST00000342175.11:c.59864A= (TTN) ENSP00000340554.6:p.Gln19955=
ENST00000359218.10:c.59663A= (TTN) ENSP00000352154.5:p.Gln19888=
ENST00000342175.10:c.59864A= (TTN) ENSP00000340554.6:p.Gln19955=
ENST00000342992.10:c.78779A= (TTN) ENSP00000343764.6:p.Gln26260=
ENST00000359218.9:c.59663A= (TTN) ENSP00000352154.5:p.Gln19888=
ENST00000460472.6:c.59288A= (TTN) ENSP00000434586.1:p.Gln19763=
ENST00000589042.5:c.86483A= (TTN) MANE Select ENSP00000467141.1:p.Gln28828=
ENST00000591111.5:c.81560A= (TTN) ENSP00000465570.1:p.Gln27187=
ENST00000615779.4:c.81560A= (TTN) ENSP00000483597.1:p.Gln27187=
NM_001256850.1:c.81560A= (TTN) NP_001243779.1:p.Gln27187=
NM_001267550.2:c.86483A= (TTN) MANE Select NP_001254479.2:p.Gln28828=
NM_003319.4:c.59288A= (TTN) NP_003310.4:p.Gln19763=
NM_133378.4:c.78779A= (TTN) NP_596869.4:p.Gln26260=
NM_133432.3:c.59663A= (TTN) NP_597676.3:p.Gln19888=
NM_133437.4:c.59864A= (TTN) NP_597681.4:p.Gln19955=
NR_038271.1:n.447-11651T= (TTN-AS1)
NR_038272.1:n.2043+17288T= (TTN-AS1)
XM_011511729.1:c.85580A= (TTN) XP_011510031.1:p.Gln28527=
XM_011511730.1:c.59474A= (TTN) XP_011510032.1:p.Gln19825=
XM_011511731.1:c.59333A= (TTN) XP_011510033.1:p.Gln19778=
XM_017004819.1:c.85376A= (TTN) XP_016860308.1:p.Gln28459=
XM_017004820.1:c.80774A= (TTN) XP_016860309.1:p.Gln26925=
XM_017004821.1:c.80771A= (TTN) XP_016860310.1:p.Gln26924=
XM_017004822.1:c.77813A= (TTN) XP_016860311.1:p.Gln25938=
XM_017004823.1:c.59429A= (TTN) XP_016860312.1:p.Gln19810=
XM_024453094.1:c.80924A= (TTN) XP_024308862.1:p.Gln26975=
XM_024453095.1:c.80921A= (TTN) XP_024308863.1:p.Gln26974=
XM_024453096.1:c.80354A= (TTN) XP_024308864.1:p.Gln26785=
XM_024453097.1:c.77696A= (TTN) XP_024308865.1:p.Gln25899=
XM_024453098.1:c.77615A= (TTN) XP_024308866.1:p.Gln25872=
XM_024453099.1:c.59378A= (TTN) XP_024308867.1:p.Gln19793=
XM_024453100.1:c.49232A= (TTN) XP_024308868.1:p.Gln16411=