Canonical Allele Identifier: CA349650320
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178632393T>A , CM000664.2:g.178632393T>A GRCh38
NC_000002.11:g.179497120T>A , CM000664.1:g.179497120T>A GRCh37
NC_000002.10:g.179205365T>A NCBI36
NG_011618.3:g.203410A>T , LRG_391:g.203410A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.35797A>T ENSP00000343764.6:p.Thr11933Ser
ENST00000342175.11:c.16882A>T ENSP00000340554.6:p.Thr5628Ser
ENST00000359218.10:c.16681A>T ENSP00000352154.5:p.Thr5561Ser
ENST00000342175.10:c.16882A>T ENSP00000340554.6:p.Thr5628Ser
ENST00000342992.10:c.35797A>T ENSP00000343764.6:p.Thr11933Ser
ENST00000359218.9:c.16681A>T ENSP00000352154.5:p.Thr5561Ser
ENST00000460472.6:c.16306A>T ENSP00000434586.1:p.Thr5436Ser
ENST00000589042.5:c.43501A>T MANE Select ENSP00000467141.1:p.Thr14501Ser
ENST00000591111.5:c.38578A>T ENSP00000465570.1:p.Thr12860Ser
ENST00000615779.4:c.38578A>T ENSP00000483597.1:p.Thr12860Ser
NM_001256850.1:c.38578A>T NP_001243779.1:p.Thr12860Ser
NM_001267550.2:c.43501A>T MANE Select NP_001254479.2:p.Thr14501Ser
NM_003319.4:c.16306A>T NP_003310.4:p.Thr5436Ser
NM_133378.4:c.35797A>T NP_596869.4:p.Thr11933Ser
NM_133432.3:c.16681A>T NP_597676.3:p.Thr5561Ser
NM_133437.4:c.16882A>T NP_597681.4:p.Thr5628Ser
XM_011511729.1:c.42598A>T XP_011510031.1:p.Thr14200Ser
XM_011511730.1:c.16492A>T XP_011510032.1:p.Thr5498Ser
XM_011511731.1:c.16351A>T XP_011510033.1:p.Thr5451Ser
XM_017004819.1:c.42394A>T XP_016860308.1:p.Thr14132Ser
XM_017004820.1:c.37792A>T XP_016860309.1:p.Thr12598Ser
XM_017004821.1:c.37789A>T XP_016860310.1:p.Thr12597Ser
XM_017004822.1:c.34831A>T XP_016860311.1:p.Thr11611Ser
XM_017004823.1:c.16447A>T XP_016860312.1:p.Thr5483Ser
XM_024453094.1:c.37942A>T XP_024308862.1:p.Thr12648Ser
XM_024453095.1:c.37939A>T XP_024308863.1:p.Thr12647Ser
XM_024453096.1:c.37372A>T XP_024308864.1:p.Thr12458Ser
XM_024453097.1:c.34714A>T XP_024308865.1:p.Thr11572Ser
XM_024453098.1:c.34633A>T XP_024308866.1:p.Thr11545Ser
XM_024453099.1:c.16396A>T XP_024308867.1:p.Thr5466Ser
XM_024453100.1:c.6250A>T XP_024308868.1:p.Thr2084Ser