Canonical Allele Identifier: CA1310518149

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532261T= , CM000664.2:g.178532261T= GRCh38
NC_000002.11:g.179396988T= , CM000664.1:g.179396988T= GRCh37
NC_000002.10:g.179105234T= NCBI36
NG_011618.3:g.303542A= , LRG_391:g.303542A=
NG_051363.1:g.14435T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96650A= (TTN) ENSP00000343764.6:p.Glu32217=
ENST00000342175.11:c.77735A= (TTN) ENSP00000340554.6:p.Glu25912=
ENST00000359218.10:c.77534A= (TTN) ENSP00000352154.5:p.Glu25845=
ENST00000342175.10:c.77735A= (TTN) ENSP00000340554.6:p.Glu25912=
ENST00000342992.10:c.96650A= (TTN) ENSP00000343764.6:p.Glu32217=
ENST00000359218.9:c.77534A= (TTN) ENSP00000352154.5:p.Glu25845=
ENST00000460472.6:c.77159A= (TTN) ENSP00000434586.1:p.Glu25720=
ENST00000589042.5:c.104354A= (TTN) MANE Select ENSP00000467141.1:p.Glu34785=
ENST00000591111.5:c.99431A= (TTN) ENSP00000465570.1:p.Glu33144=
ENST00000615779.4:c.99431A= (TTN) ENSP00000483597.1:p.Glu33144=
NM_001256850.1:c.99431A= (TTN) NP_001243779.1:p.Glu33144=
NM_001267550.2:c.104354A= (TTN) MANE Select NP_001254479.2:p.Glu34785=
NM_003319.4:c.77159A= (TTN) NP_003310.4:p.Glu25720=
NM_133378.4:c.96650A= (TTN) NP_596869.4:p.Glu32217=
NM_133432.3:c.77534A= (TTN) NP_597676.3:p.Glu25845=
NM_133437.4:c.77735A= (TTN) NP_597681.4:p.Glu25912=
NR_038271.1:n.446+8625T= (TTN-AS1)
NR_038272.1:n.220-3471T= (TTN-AS1)
XM_011511729.1:c.103451A= (TTN) XP_011510031.1:p.Glu34484=
XM_011511730.1:c.77345A= (TTN) XP_011510032.1:p.Glu25782=
XM_011511731.1:c.77204A= (TTN) XP_011510033.1:p.Glu25735=
XM_017004819.1:c.103247A= (TTN) XP_016860308.1:p.Glu34416=
XM_017004820.1:c.98645A= (TTN) XP_016860309.1:p.Glu32882=
XM_017004821.1:c.98642A= (TTN) XP_016860310.1:p.Glu32881=
XM_017004822.1:c.95684A= (TTN) XP_016860311.1:p.Glu31895=
XM_017004823.1:c.77300A= (TTN) XP_016860312.1:p.Glu25767=
XM_024453094.1:c.98795A= (TTN) XP_024308862.1:p.Glu32932=
XM_024453095.1:c.98792A= (TTN) XP_024308863.1:p.Glu32931=
XM_024453096.1:c.98225A= (TTN) XP_024308864.1:p.Glu32742=
XM_024453097.1:c.95567A= (TTN) XP_024308865.1:p.Glu31856=
XM_024453098.1:c.95486A= (TTN) XP_024308866.1:p.Glu31829=
XM_024453099.1:c.77249A= (TTN) XP_024308867.1:p.Glu25750=
XM_024453100.1:c.67103A= (TTN) XP_024308868.1:p.Glu22368=