Canonical Allele Identifier: CA430275751
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178620258T>A , CM000664.2:g.178620258T>A GRCh38
NC_000002.11:g.179484985T>A , CM000664.1:g.179484985T>A GRCh37
NC_000002.10:g.179193230T>A NCBI36
NG_011618.3:g.215545A>T , LRG_391:g.215545A>T
NG_051363.1:g.102432T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.38559A>T ENSP00000343764.6:p.Val12853=
ENST00000342175.11:c.19644A>T ENSP00000340554.6:p.Val6548=
ENST00000359218.10:c.19443A>T ENSP00000352154.5:p.Val6481=
ENST00000342175.10:c.19644A>T ENSP00000340554.6:p.Val6548=
ENST00000342992.10:c.38559A>T ENSP00000343764.6:p.Val12853=
ENST00000359218.9:c.19443A>T ENSP00000352154.5:p.Val6481=
ENST00000460472.6:c.19068A>T ENSP00000434586.1:p.Val6356=
ENST00000589042.5:c.46263A>T MANE Select ENSP00000467141.1:p.Val15421=
ENST00000591111.5:c.41340A>T ENSP00000465570.1:p.Val13780=
ENST00000615779.4:c.41340A>T ENSP00000483597.1:p.Val13780=
NM_001256850.1:c.41340A>T NP_001243779.1:p.Val13780=
NM_001267550.2:c.46263A>T MANE Select NP_001254479.2:p.Val15421=
NM_003319.4:c.19068A>T NP_003310.4:p.Val6356=
NM_133378.4:c.38559A>T NP_596869.4:p.Val12853=
NM_133432.3:c.19443A>T NP_597676.3:p.Val6481=
NM_133437.4:c.19644A>T NP_597681.4:p.Val6548=
XM_011511729.1:c.45360A>T XP_011510031.1:p.Val15120=
XM_011511730.1:c.19254A>T XP_011510032.1:p.Val6418=
XM_011511731.1:c.19113A>T XP_011510033.1:p.Val6371=
XM_017004819.1:c.45156A>T XP_016860308.1:p.Val15052=
XM_017004820.1:c.40554A>T XP_016860309.1:p.Val13518=
XM_017004821.1:c.40551A>T XP_016860310.1:p.Val13517=
XM_017004822.1:c.37593A>T XP_016860311.1:p.Val12531=
XM_017004823.1:c.19209A>T XP_016860312.1:p.Val6403=
XM_024453094.1:c.40704A>T XP_024308862.1:p.Val13568=
XM_024453095.1:c.40701A>T XP_024308863.1:p.Val13567=
XM_024453096.1:c.40134A>T XP_024308864.1:p.Val13378=
XM_024453097.1:c.37476A>T XP_024308865.1:p.Val12492=
XM_024453098.1:c.37395A>T XP_024308866.1:p.Val12465=
XM_024453099.1:c.19158A>T XP_024308867.1:p.Val6386=
XM_024453100.1:c.9012A>T XP_024308868.1:p.Val3004=