Canonical Allele Identifier: CA353111
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 223274
dbSNP Id: rs869312043

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178636098G>A , CM000664.2:g.178636098G>A GRCh38
NC_000002.11:g.179500825G>A , CM000664.1:g.179500825G>A GRCh37
NC_000002.10:g.179209070G>A NCBI36
NG_011618.3:g.199705C>T , LRG_391:g.199705C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.33769C>T ENSP00000343764.6:p.Arg11257Ter
ENST00000342175.11:c.14854C>T ENSP00000340554.6:p.Arg4952Ter
ENST00000359218.10:c.14653C>T ENSP00000352154.5:p.Arg4885Ter
ENST00000342175.10:c.14854C>T ENSP00000340554.6:p.Arg4952Ter
ENST00000342992.10:c.33769C>T ENSP00000343764.6:p.Arg11257Ter
ENST00000359218.9:c.14653C>T ENSP00000352154.5:p.Arg4885Ter
ENST00000460472.6:c.14278C>T ENSP00000434586.1:p.Arg4760Ter
ENST00000589042.5:c.41473C>T MANE Select ENSP00000467141.1:p.Arg13825Ter
ENST00000591111.5:c.36550C>T ENSP00000465570.1:p.Arg12184Ter
ENST00000615779.4:c.36550C>T ENSP00000483597.1:p.Arg12184Ter
NM_001256850.1:c.36550C>T NP_001243779.1:p.Arg12184Ter
NM_001267550.2:c.41473C>T MANE Select NP_001254479.2:p.Arg13825Ter
NM_003319.4:c.14278C>T NP_003310.4:p.Arg4760Ter
NM_133378.4:c.33769C>T NP_596869.4:p.Arg11257Ter
NM_133432.3:c.14653C>T NP_597676.3:p.Arg4885Ter
NM_133437.4:c.14854C>T NP_597681.4:p.Arg4952Ter
XM_011511729.1:c.40570C>T XP_011510031.1:p.Arg13524Ter
XM_011511730.1:c.14464C>T XP_011510032.1:p.Arg4822Ter
XM_011511731.1:c.14323C>T XP_011510033.1:p.Arg4775Ter
XM_017004819.1:c.40366C>T XP_016860308.1:p.Arg13456Ter
XM_017004820.1:c.35764C>T XP_016860309.1:p.Arg11922Ter
XM_017004821.1:c.35761C>T XP_016860310.1:p.Arg11921Ter
XM_017004822.1:c.32803C>T XP_016860311.1:p.Arg10935Ter
XM_017004823.1:c.14419C>T XP_016860312.1:p.Arg4807Ter
XM_024453094.1:c.35914C>T XP_024308862.1:p.Arg11972Ter
XM_024453095.1:c.35911C>T XP_024308863.1:p.Arg11971Ter
XM_024453096.1:c.35344C>T XP_024308864.1:p.Arg11782Ter
XM_024453097.1:c.32686C>T XP_024308865.1:p.Arg10896Ter
XM_024453098.1:c.32605C>T XP_024308866.1:p.Arg10869Ter
XM_024453099.1:c.14368C>T XP_024308867.1:p.Arg4790Ter
XM_024453100.1:c.4222C>T XP_024308868.1:p.Arg1408Ter