Canonical Allele Identifier: CA1310556247
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631156G= , CM000664.2:g.178631156G= GRCh38
NC_000002.11:g.179495883G= , CM000664.1:g.179495883G= GRCh37
NC_000002.10:g.179204128G= NCBI36
NG_011618.3:g.204647C= , LRG_391:g.204647C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36188C= ENSP00000343764.6:p.Ala12063=
ENST00000342175.11:c.17273C= ENSP00000340554.6:p.Ala5758=
ENST00000359218.10:c.17072C= ENSP00000352154.5:p.Ala5691=
ENST00000342175.10:c.17273C= ENSP00000340554.6:p.Ala5758=
ENST00000342992.10:c.36188C= ENSP00000343764.6:p.Ala12063=
ENST00000359218.9:c.17072C= ENSP00000352154.5:p.Ala5691=
ENST00000460472.6:c.16697C= ENSP00000434586.1:p.Ala5566=
ENST00000589042.5:c.43892C= MANE Select ENSP00000467141.1:p.Ala14631=
ENST00000591111.5:c.38969C= ENSP00000465570.1:p.Ala12990=
ENST00000615779.4:c.38969C= ENSP00000483597.1:p.Ala12990=
NM_001256850.1:c.38969C= NP_001243779.1:p.Ala12990=
NM_001267550.2:c.43892C= MANE Select NP_001254479.2:p.Ala14631=
NM_003319.4:c.16697C= NP_003310.4:p.Ala5566=
NM_133378.4:c.36188C= NP_596869.4:p.Ala12063=
NM_133432.3:c.17072C= NP_597676.3:p.Ala5691=
NM_133437.4:c.17273C= NP_597681.4:p.Ala5758=
XM_011511729.1:c.42989C= XP_011510031.1:p.Ala14330=
XM_011511730.1:c.16883C= XP_011510032.1:p.Ala5628=
XM_011511731.1:c.16742C= XP_011510033.1:p.Ala5581=
XM_017004819.1:c.42785C= XP_016860308.1:p.Ala14262=
XM_017004820.1:c.38183C= XP_016860309.1:p.Ala12728=
XM_017004821.1:c.38180C= XP_016860310.1:p.Ala12727=
XM_017004822.1:c.35222C= XP_016860311.1:p.Ala11741=
XM_017004823.1:c.16838C= XP_016860312.1:p.Ala5613=
XM_024453094.1:c.38333C= XP_024308862.1:p.Ala12778=
XM_024453095.1:c.38330C= XP_024308863.1:p.Ala12777=
XM_024453096.1:c.37763C= XP_024308864.1:p.Ala12588=
XM_024453097.1:c.35105C= XP_024308865.1:p.Ala11702=
XM_024453098.1:c.35024C= XP_024308866.1:p.Ala11675=
XM_024453099.1:c.16787C= XP_024308867.1:p.Ala5596=
XM_024453100.1:c.6641C= XP_024308868.1:p.Ala2214=