Canonical Allele Identifier: CA1310530434

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178569422A= , CM000664.2:g.178569422A= GRCh38
NC_000002.11:g.179434149A= , CM000664.1:g.179434149A= GRCh37
NC_000002.10:g.179142395A= NCBI36
NG_011618.3:g.266381T= , LRG_391:g.266381T=
NG_051363.1:g.51596A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69006T= (TTN) ENSP00000343764.6:p.Asn23002=
ENST00000342175.11:c.50091T= (TTN) ENSP00000340554.6:p.Asn16697=
ENST00000359218.10:c.49890T= (TTN) ENSP00000352154.5:p.Asn16630=
ENST00000342175.10:c.50091T= (TTN) ENSP00000340554.6:p.Asn16697=
ENST00000342992.10:c.69006T= (TTN) ENSP00000343764.6:p.Asn23002=
ENST00000359218.9:c.49890T= (TTN) ENSP00000352154.5:p.Asn16630=
ENST00000460472.6:c.49515T= (TTN) ENSP00000434586.1:p.Asn16505=
ENST00000589042.5:c.76710T= (TTN) MANE Select ENSP00000467141.1:p.Asn25570=
ENST00000591111.5:c.71787T= (TTN) ENSP00000465570.1:p.Asn23929=
ENST00000615779.4:c.71787T= (TTN) ENSP00000483597.1:p.Asn23929=
NM_001256850.1:c.71787T= (TTN) NP_001243779.1:p.Asn23929=
NM_001267550.2:c.76710T= (TTN) MANE Select NP_001254479.2:p.Asn25570=
NM_003319.4:c.49515T= (TTN) NP_003310.4:p.Asn16505=
NM_133378.4:c.69006T= (TTN) NP_596869.4:p.Asn23002=
NM_133432.3:c.49890T= (TTN) NP_597676.3:p.Asn16630=
NM_133437.4:c.50091T= (TTN) NP_597681.4:p.Asn16697=
NR_038271.1:n.447-1878A= (TTN-AS1)
NR_038272.1:n.2044-13150A= (TTN-AS1)
XM_011511729.1:c.75807T= (TTN) XP_011510031.1:p.Asn25269=
XM_011511730.1:c.49701T= (TTN) XP_011510032.1:p.Asn16567=
XM_011511731.1:c.49560T= (TTN) XP_011510033.1:p.Asn16520=
XM_017004819.1:c.75603T= (TTN) XP_016860308.1:p.Asn25201=
XM_017004820.1:c.71001T= (TTN) XP_016860309.1:p.Asn23667=
XM_017004821.1:c.70998T= (TTN) XP_016860310.1:p.Asn23666=
XM_017004822.1:c.68040T= (TTN) XP_016860311.1:p.Asn22680=
XM_017004823.1:c.49656T= (TTN) XP_016860312.1:p.Asn16552=
XM_024453094.1:c.71151T= (TTN) XP_024308862.1:p.Asn23717=
XM_024453095.1:c.71148T= (TTN) XP_024308863.1:p.Asn23716=
XM_024453096.1:c.70581T= (TTN) XP_024308864.1:p.Asn23527=
XM_024453097.1:c.67923T= (TTN) XP_024308865.1:p.Asn22641=
XM_024453098.1:c.67842T= (TTN) XP_024308866.1:p.Asn22614=
XM_024453099.1:c.49605T= (TTN) XP_024308867.1:p.Asn16535=
XM_024453100.1:c.39459T= (TTN) XP_024308868.1:p.Asn13153=