Canonical Allele Identifier: CA1310514702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530511A= , CM000664.2:g.178530511A= GRCh38
NC_000002.11:g.179395238A= , CM000664.1:g.179395238A= GRCh37
NC_000002.10:g.179103484A= NCBI36
NG_011618.3:g.305292T= , LRG_391:g.305292T=
NG_051363.1:g.12685A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98400T= (TTN) ENSP00000343764.6:p.Ser32800=
ENST00000342175.11:c.79485T= (TTN) ENSP00000340554.6:p.Ser26495=
ENST00000359218.10:c.79284T= (TTN) ENSP00000352154.5:p.Ser26428=
ENST00000342175.10:c.79485T= (TTN) ENSP00000340554.6:p.Ser26495=
ENST00000342992.10:c.98400T= (TTN) ENSP00000343764.6:p.Ser32800=
ENST00000359218.9:c.79284T= (TTN) ENSP00000352154.5:p.Ser26428=
ENST00000460472.6:c.78909T= (TTN) ENSP00000434586.1:p.Ser26303=
ENST00000589042.5:c.106104T= (TTN) MANE Select ENSP00000467141.1:p.Ser35368=
ENST00000591111.5:c.101181T= (TTN) ENSP00000465570.1:p.Ser33727=
ENST00000615779.4:c.101181T= (TTN) ENSP00000483597.1:p.Ser33727=
NM_001256850.1:c.101181T= (TTN) NP_001243779.1:p.Ser33727=
NM_001267550.2:c.106104T= (TTN) MANE Select NP_001254479.2:p.Ser35368=
NM_003319.4:c.78909T= (TTN) NP_003310.4:p.Ser26303=
NM_133378.4:c.98400T= (TTN) NP_596869.4:p.Ser32800=
NM_133432.3:c.79284T= (TTN) NP_597676.3:p.Ser26428=
NM_133437.4:c.79485T= (TTN) NP_597681.4:p.Ser26495=
NR_038271.1:n.446+6875A= (TTN-AS1)
NR_038272.1:n.220-5221A= (TTN-AS1)
XM_011511729.1:c.105201T= (TTN) XP_011510031.1:p.Ser35067=
XM_011511730.1:c.79095T= (TTN) XP_011510032.1:p.Ser26365=
XM_011511731.1:c.78954T= (TTN) XP_011510033.1:p.Ser26318=
XM_017004819.1:c.104997T= (TTN) XP_016860308.1:p.Ser34999=
XM_017004820.1:c.100395T= (TTN) XP_016860309.1:p.Ser33465=
XM_017004821.1:c.100392T= (TTN) XP_016860310.1:p.Ser33464=
XM_017004822.1:c.97434T= (TTN) XP_016860311.1:p.Ser32478=
XM_017004823.1:c.79050T= (TTN) XP_016860312.1:p.Ser26350=
XM_024453094.1:c.100545T= (TTN) XP_024308862.1:p.Ser33515=
XM_024453095.1:c.100542T= (TTN) XP_024308863.1:p.Ser33514=
XM_024453096.1:c.99975T= (TTN) XP_024308864.1:p.Ser33325=
XM_024453097.1:c.97317T= (TTN) XP_024308865.1:p.Ser32439=
XM_024453098.1:c.97236T= (TTN) XP_024308866.1:p.Ser32412=
XM_024453099.1:c.78999T= (TTN) XP_024308867.1:p.Ser26333=
XM_024453100.1:c.68853T= (TTN) XP_024308868.1:p.Ser22951=