Canonical Allele Identifier: CA1310514506

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530310A= , CM000664.2:g.178530310A= GRCh38
NC_000002.11:g.179395037A= , CM000664.1:g.179395037A= GRCh37
NC_000002.10:g.179103283A= NCBI36
NG_011618.3:g.305493T= , LRG_391:g.305493T=
NG_051363.1:g.12484A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98601T= (TTN) ENSP00000343764.6:p.Ser32867=
ENST00000342175.11:c.79686T= (TTN) ENSP00000340554.6:p.Ser26562=
ENST00000359218.10:c.79485T= (TTN) ENSP00000352154.5:p.Ser26495=
ENST00000342175.10:c.79686T= (TTN) ENSP00000340554.6:p.Ser26562=
ENST00000342992.10:c.98601T= (TTN) ENSP00000343764.6:p.Ser32867=
ENST00000359218.9:c.79485T= (TTN) ENSP00000352154.5:p.Ser26495=
ENST00000460472.6:c.79110T= (TTN) ENSP00000434586.1:p.Ser26370=
ENST00000589042.5:c.106305T= (TTN) MANE Select ENSP00000467141.1:p.Ser35435=
ENST00000591111.5:c.101382T= (TTN) ENSP00000465570.1:p.Ser33794=
ENST00000615779.4:c.101382T= (TTN) ENSP00000483597.1:p.Ser33794=
NM_001256850.1:c.101382T= (TTN) NP_001243779.1:p.Ser33794=
NM_001267550.2:c.106305T= (TTN) MANE Select NP_001254479.2:p.Ser35435=
NM_003319.4:c.79110T= (TTN) NP_003310.4:p.Ser26370=
NM_133378.4:c.98601T= (TTN) NP_596869.4:p.Ser32867=
NM_133432.3:c.79485T= (TTN) NP_597676.3:p.Ser26495=
NM_133437.4:c.79686T= (TTN) NP_597681.4:p.Ser26562=
NR_038271.1:n.446+6674A= (TTN-AS1)
NR_038272.1:n.220-5422A= (TTN-AS1)
XM_011511729.1:c.105402T= (TTN) XP_011510031.1:p.Ser35134=
XM_011511730.1:c.79296T= (TTN) XP_011510032.1:p.Ser26432=
XM_011511731.1:c.79155T= (TTN) XP_011510033.1:p.Ser26385=
XM_017004819.1:c.105198T= (TTN) XP_016860308.1:p.Ser35066=
XM_017004820.1:c.100596T= (TTN) XP_016860309.1:p.Ser33532=
XM_017004821.1:c.100593T= (TTN) XP_016860310.1:p.Ser33531=
XM_017004822.1:c.97635T= (TTN) XP_016860311.1:p.Ser32545=
XM_017004823.1:c.79251T= (TTN) XP_016860312.1:p.Ser26417=
XM_024453094.1:c.100746T= (TTN) XP_024308862.1:p.Ser33582=
XM_024453095.1:c.100743T= (TTN) XP_024308863.1:p.Ser33581=
XM_024453096.1:c.100176T= (TTN) XP_024308864.1:p.Ser33392=
XM_024453097.1:c.97518T= (TTN) XP_024308865.1:p.Ser32506=
XM_024453098.1:c.97437T= (TTN) XP_024308866.1:p.Ser32479=
XM_024453099.1:c.79200T= (TTN) XP_024308867.1:p.Ser26400=
XM_024453100.1:c.69054T= (TTN) XP_024308868.1:p.Ser23018=