Canonical Allele Identifier: CA1310555897
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630242C= , CM000664.2:g.178630242C= GRCh38
NC_000002.11:g.179494969C= , CM000664.1:g.179494969C= GRCh37
NC_000002.10:g.179203214C= NCBI36
NG_011618.3:g.205561G= , LRG_391:g.205561G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36576G= ENSP00000343764.6:p.Lys12192=
ENST00000342175.11:c.17661G= ENSP00000340554.6:p.Lys5887=
ENST00000359218.10:c.17460G= ENSP00000352154.5:p.Lys5820=
ENST00000342175.10:c.17661G= ENSP00000340554.6:p.Lys5887=
ENST00000342992.10:c.36576G= ENSP00000343764.6:p.Lys12192=
ENST00000359218.9:c.17460G= ENSP00000352154.5:p.Lys5820=
ENST00000460472.6:c.17085G= ENSP00000434586.1:p.Lys5695=
ENST00000589042.5:c.44280G= MANE Select ENSP00000467141.1:p.Lys14760=
ENST00000591111.5:c.39357G= ENSP00000465570.1:p.Lys13119=
ENST00000615779.4:c.39357G= ENSP00000483597.1:p.Lys13119=
NM_001256850.1:c.39357G= NP_001243779.1:p.Lys13119=
NM_001267550.2:c.44280G= MANE Select NP_001254479.2:p.Lys14760=
NM_003319.4:c.17085G= NP_003310.4:p.Lys5695=
NM_133378.4:c.36576G= NP_596869.4:p.Lys12192=
NM_133432.3:c.17460G= NP_597676.3:p.Lys5820=
NM_133437.4:c.17661G= NP_597681.4:p.Lys5887=
XM_011511729.1:c.43377G= XP_011510031.1:p.Lys14459=
XM_011511730.1:c.17271G= XP_011510032.1:p.Lys5757=
XM_011511731.1:c.17130G= XP_011510033.1:p.Lys5710=
XM_017004819.1:c.43173G= XP_016860308.1:p.Lys14391=
XM_017004820.1:c.38571G= XP_016860309.1:p.Lys12857=
XM_017004821.1:c.38568G= XP_016860310.1:p.Lys12856=
XM_017004822.1:c.35610G= XP_016860311.1:p.Lys11870=
XM_017004823.1:c.17226G= XP_016860312.1:p.Lys5742=
XM_024453094.1:c.38721G= XP_024308862.1:p.Lys12907=
XM_024453095.1:c.38718G= XP_024308863.1:p.Lys12906=
XM_024453096.1:c.38151G= XP_024308864.1:p.Lys12717=
XM_024453097.1:c.35493G= XP_024308865.1:p.Lys11831=
XM_024453098.1:c.35412G= XP_024308866.1:p.Lys11804=
XM_024453099.1:c.17175G= XP_024308867.1:p.Lys5725=
XM_024453100.1:c.7029G= XP_024308868.1:p.Lys2343=