Canonical Allele Identifier: CA1310514623

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530427A= , CM000664.2:g.178530427A= GRCh38
NC_000002.11:g.179395154A= , CM000664.1:g.179395154A= GRCh37
NC_000002.10:g.179103400A= NCBI36
NG_011618.3:g.305376T= , LRG_391:g.305376T=
NG_051363.1:g.12601A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98484T= (TTN) ENSP00000343764.6:p.Asp32828=
ENST00000342175.11:c.79569T= (TTN) ENSP00000340554.6:p.Asp26523=
ENST00000359218.10:c.79368T= (TTN) ENSP00000352154.5:p.Asp26456=
ENST00000342175.10:c.79569T= (TTN) ENSP00000340554.6:p.Asp26523=
ENST00000342992.10:c.98484T= (TTN) ENSP00000343764.6:p.Asp32828=
ENST00000359218.9:c.79368T= (TTN) ENSP00000352154.5:p.Asp26456=
ENST00000460472.6:c.78993T= (TTN) ENSP00000434586.1:p.Asp26331=
ENST00000589042.5:c.106188T= (TTN) MANE Select ENSP00000467141.1:p.Asp35396=
ENST00000591111.5:c.101265T= (TTN) ENSP00000465570.1:p.Asp33755=
ENST00000615779.4:c.101265T= (TTN) ENSP00000483597.1:p.Asp33755=
NM_001256850.1:c.101265T= (TTN) NP_001243779.1:p.Asp33755=
NM_001267550.2:c.106188T= (TTN) MANE Select NP_001254479.2:p.Asp35396=
NM_003319.4:c.78993T= (TTN) NP_003310.4:p.Asp26331=
NM_133378.4:c.98484T= (TTN) NP_596869.4:p.Asp32828=
NM_133432.3:c.79368T= (TTN) NP_597676.3:p.Asp26456=
NM_133437.4:c.79569T= (TTN) NP_597681.4:p.Asp26523=
NR_038271.1:n.446+6791A= (TTN-AS1)
NR_038272.1:n.220-5305A= (TTN-AS1)
XM_011511729.1:c.105285T= (TTN) XP_011510031.1:p.Asp35095=
XM_011511730.1:c.79179T= (TTN) XP_011510032.1:p.Asp26393=
XM_011511731.1:c.79038T= (TTN) XP_011510033.1:p.Asp26346=
XM_017004819.1:c.105081T= (TTN) XP_016860308.1:p.Asp35027=
XM_017004820.1:c.100479T= (TTN) XP_016860309.1:p.Asp33493=
XM_017004821.1:c.100476T= (TTN) XP_016860310.1:p.Asp33492=
XM_017004822.1:c.97518T= (TTN) XP_016860311.1:p.Asp32506=
XM_017004823.1:c.79134T= (TTN) XP_016860312.1:p.Asp26378=
XM_024453094.1:c.100629T= (TTN) XP_024308862.1:p.Asp33543=
XM_024453095.1:c.100626T= (TTN) XP_024308863.1:p.Asp33542=
XM_024453096.1:c.100059T= (TTN) XP_024308864.1:p.Asp33353=
XM_024453097.1:c.97401T= (TTN) XP_024308865.1:p.Asp32467=
XM_024453098.1:c.97320T= (TTN) XP_024308866.1:p.Asp32440=
XM_024453099.1:c.79083T= (TTN) XP_024308867.1:p.Asp26361=
XM_024453100.1:c.68937T= (TTN) XP_024308868.1:p.Asp22979=