Canonical Allele Identifier: CA2005349
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 393026
dbSNP Id: rs746063269

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178777910G>A , CM000664.2:g.178777910G>A GRCh38
NC_000002.11:g.179642637G>A , CM000664.1:g.179642637G>A GRCh37
NC_000002.10:g.179350882G>A NCBI36
NG_011618.3:g.57893C>T , LRG_391:g.57893C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.4274C>T ENSP00000343764.6:p.Ala1425Val
ENST00000342175.11:c.4136C>T ENSP00000340554.6:p.Ala1379Val
ENST00000359218.10:c.4136C>T ENSP00000352154.5:p.Ala1379Val
ENST00000360870.10:c.4274C>T MANE Plus Clinical ENSP00000354117.4:p.Ala1425Val
ENST00000342175.10:c.4136C>T ENSP00000340554.6:p.Ala1379Val
ENST00000342992.10:c.4274C>T ENSP00000343764.6:p.Ala1425Val
ENST00000359218.9:c.4136C>T ENSP00000352154.5:p.Ala1379Val
ENST00000360870.9:c.4274C>T ENSP00000354117.4:p.Ala1425Val
ENST00000460472.6:c.4136C>T ENSP00000434586.1:p.Ala1379Val
ENST00000589042.5:c.4274C>T MANE Select ENSP00000467141.1:p.Ala1425Val
ENST00000591111.5:c.4274C>T ENSP00000465570.1:p.Ala1425Val
ENST00000615779.4:c.4274C>T ENSP00000483597.1:p.Ala1425Val
NM_001256850.1:c.4274C>T NP_001243779.1:p.Ala1425Val
NM_001267550.2:c.4274C>T MANE Select NP_001254479.2:p.Ala1425Val
NM_003319.4:c.4136C>T NP_003310.4:p.Ala1379Val
NM_133378.4:c.4274C>T NP_596869.4:p.Ala1425Val
NM_133379.4:c.4274C>T , LRG_391t2:c.4274C>T NP_596870.2:p.Ala1425Val
NM_133432.3:c.4136C>T NP_597676.3:p.Ala1379Val
NM_133437.4:c.4136C>T NP_597681.4:p.Ala1379Val
NR_120594.1:n.985G>A
XM_011511729.1:c.4322C>T XP_011510031.1:p.Ala1441Val
XM_011511730.1:c.4322C>T XP_011510032.1:p.Ala1441Val
XM_011511731.1:c.4181C>T XP_011510033.1:p.Ala1394Val
XM_011511732.1:c.4319C>T XP_011510034.1:p.Ala1440Val
XM_017004819.1:c.4277C>T XP_016860308.1:p.Ala1426Val
XM_017004820.1:c.4277C>T XP_016860309.1:p.Ala1426Val
XM_017004821.1:c.4274C>T XP_016860310.1:p.Ala1425Val
XM_017004822.1:c.4277C>T XP_016860311.1:p.Ala1426Val
XM_017004823.1:c.4277C>T XP_016860312.1:p.Ala1426Val
XM_024453094.1:c.4277C>T XP_024308862.1:p.Ala1426Val
XM_024453095.1:c.4277C>T XP_024308863.1:p.Ala1426Val
XM_024453096.1:c.4277C>T XP_024308864.1:p.Ala1426Val
XM_024453097.1:c.4277C>T XP_024308865.1:p.Ala1426Val
XM_024453098.1:c.4277C>T XP_024308866.1:p.Ala1426Val
XM_024453099.1:c.4277C>T XP_024308867.1:p.Ala1426Val
NM_133379.5:c.4274C>T MANE Plus Clinical NP_596870.2:p.Ala1425Val