Canonical Allele Identifier: CA1310540448

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178593237T= , CM000664.2:g.178593237T= GRCh38
NC_000002.11:g.179457964T= , CM000664.1:g.179457964T= GRCh37
NC_000002.10:g.179166210T= NCBI36
NG_011618.3:g.242566A= , LRG_391:g.242566A=
NG_051363.1:g.75411T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.51267A= (TTN) ENSP00000343764.6:p.Glu17089=
ENST00000342175.11:c.32352A= (TTN) ENSP00000340554.6:p.Glu10784=
ENST00000359218.10:c.32151A= (TTN) ENSP00000352154.5:p.Glu10717=
ENST00000342175.10:c.32352A= (TTN) ENSP00000340554.6:p.Glu10784=
ENST00000342992.10:c.51267A= (TTN) ENSP00000343764.6:p.Glu17089=
ENST00000359218.9:c.32151A= (TTN) ENSP00000352154.5:p.Glu10717=
ENST00000460472.6:c.31776A= (TTN) ENSP00000434586.1:p.Glu10592=
ENST00000589042.5:c.58971A= (TTN) MANE Select ENSP00000467141.1:p.Glu19657=
ENST00000591111.5:c.54048A= (TTN) ENSP00000465570.1:p.Glu18016=
ENST00000615779.4:c.54048A= (TTN) ENSP00000483597.1:p.Glu18016=
NM_001256850.1:c.54048A= (TTN) NP_001243779.1:p.Glu18016=
NM_001267550.2:c.58971A= (TTN) MANE Select NP_001254479.2:p.Glu19657=
NM_003319.4:c.31776A= (TTN) NP_003310.4:p.Glu10592=
NM_133378.4:c.51267A= (TTN) NP_596869.4:p.Glu17089=
NM_133432.3:c.32151A= (TTN) NP_597676.3:p.Glu10717=
NM_133437.4:c.32352A= (TTN) NP_597681.4:p.Glu10784=
NR_038271.1:n.597-4359T= (TTN-AS1)
NR_038272.1:n.3364+1923T= (TTN-AS1)
XM_011511729.1:c.58068A= (TTN) XP_011510031.1:p.Glu19356=
XM_011511730.1:c.31962A= (TTN) XP_011510032.1:p.Glu10654=
XM_011511731.1:c.31821A= (TTN) XP_011510033.1:p.Glu10607=
XM_017004819.1:c.57864A= (TTN) XP_016860308.1:p.Glu19288=
XM_017004820.1:c.53262A= (TTN) XP_016860309.1:p.Glu17754=
XM_017004821.1:c.53259A= (TTN) XP_016860310.1:p.Glu17753=
XM_017004822.1:c.50301A= (TTN) XP_016860311.1:p.Glu16767=
XM_017004823.1:c.31917A= (TTN) XP_016860312.1:p.Glu10639=
XM_024453094.1:c.53412A= (TTN) XP_024308862.1:p.Glu17804=
XM_024453095.1:c.53409A= (TTN) XP_024308863.1:p.Glu17803=
XM_024453096.1:c.52842A= (TTN) XP_024308864.1:p.Glu17614=
XM_024453097.1:c.50184A= (TTN) XP_024308865.1:p.Glu16728=
XM_024453098.1:c.50103A= (TTN) XP_024308866.1:p.Glu16701=
XM_024453099.1:c.31866A= (TTN) XP_024308867.1:p.Glu10622=
XM_024453100.1:c.21720A= (TTN) XP_024308868.1:p.Glu7240=