Canonical Allele Identifier: CA1310514747

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530558C= , CM000664.2:g.178530558C= GRCh38
NC_000002.11:g.179395285C= , CM000664.1:g.179395285C= GRCh37
NC_000002.10:g.179103531C= NCBI36
NG_011618.3:g.305245G= , LRG_391:g.305245G=
NG_051363.1:g.12732C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98353G= (TTN) ENSP00000343764.6:p.Asp32785=
ENST00000342175.11:c.79438G= (TTN) ENSP00000340554.6:p.Asp26480=
ENST00000359218.10:c.79237G= (TTN) ENSP00000352154.5:p.Asp26413=
ENST00000342175.10:c.79438G= (TTN) ENSP00000340554.6:p.Asp26480=
ENST00000342992.10:c.98353G= (TTN) ENSP00000343764.6:p.Asp32785=
ENST00000359218.9:c.79237G= (TTN) ENSP00000352154.5:p.Asp26413=
ENST00000460472.6:c.78862G= (TTN) ENSP00000434586.1:p.Asp26288=
ENST00000589042.5:c.106057G= (TTN) MANE Select ENSP00000467141.1:p.Asp35353=
ENST00000591111.5:c.101134G= (TTN) ENSP00000465570.1:p.Asp33712=
ENST00000615779.4:c.101134G= (TTN) ENSP00000483597.1:p.Asp33712=
NM_001256850.1:c.101134G= (TTN) NP_001243779.1:p.Asp33712=
NM_001267550.2:c.106057G= (TTN) MANE Select NP_001254479.2:p.Asp35353=
NM_003319.4:c.78862G= (TTN) NP_003310.4:p.Asp26288=
NM_133378.4:c.98353G= (TTN) NP_596869.4:p.Asp32785=
NM_133432.3:c.79237G= (TTN) NP_597676.3:p.Asp26413=
NM_133437.4:c.79438G= (TTN) NP_597681.4:p.Asp26480=
NR_038271.1:n.446+6922C= (TTN-AS1)
NR_038272.1:n.220-5174C= (TTN-AS1)
XM_011511729.1:c.105154G= (TTN) XP_011510031.1:p.Asp35052=
XM_011511730.1:c.79048G= (TTN) XP_011510032.1:p.Asp26350=
XM_011511731.1:c.78907G= (TTN) XP_011510033.1:p.Asp26303=
XM_017004819.1:c.104950G= (TTN) XP_016860308.1:p.Asp34984=
XM_017004820.1:c.100348G= (TTN) XP_016860309.1:p.Asp33450=
XM_017004821.1:c.100345G= (TTN) XP_016860310.1:p.Asp33449=
XM_017004822.1:c.97387G= (TTN) XP_016860311.1:p.Asp32463=
XM_017004823.1:c.79003G= (TTN) XP_016860312.1:p.Asp26335=
XM_024453094.1:c.100498G= (TTN) XP_024308862.1:p.Asp33500=
XM_024453095.1:c.100495G= (TTN) XP_024308863.1:p.Asp33499=
XM_024453096.1:c.99928G= (TTN) XP_024308864.1:p.Asp33310=
XM_024453097.1:c.97270G= (TTN) XP_024308865.1:p.Asp32424=
XM_024453098.1:c.97189G= (TTN) XP_024308866.1:p.Asp32397=
XM_024453099.1:c.78952G= (TTN) XP_024308867.1:p.Asp26318=
XM_024453100.1:c.68806G= (TTN) XP_024308868.1:p.Asp22936=