Canonical Allele Identifier: CA1310567280
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178658817T= , CM000664.2:g.178658817T= GRCh38
NC_000002.11:g.179523544T= , CM000664.1:g.179523544T= GRCh37
NC_000002.10:g.179231789T= NCBI36
NG_011618.3:g.176986A= , LRG_391:g.176986A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.31741+188A= ENSP00000343764.6:n.31741+188A=
ENST00000342175.11:c.13859-16500A= ENSP00000340554.6:n.13859-16500A=
ENST00000359218.10:c.13658-16500A= ENSP00000352154.5:n.13658-16500A=
ENST00000342175.10:c.13859-16500A= ENSP00000340554.6:n.13859-16500A=
ENST00000342992.10:c.31741+188A= ENSP00000343764.6:n.31741+188A=
ENST00000359218.9:c.13658-16500A= ENSP00000352154.5:n.13658-16500A=
ENST00000414766.5:c.2440+14816A= ENSP00000401501.1:n.2440+14816A=
ENST00000460472.6:c.13283-16500A= ENSP00000434586.1:n.13283-16500A=
ENST00000589042.5:c.37454-23A= MANE Select ENSP00000467141.1:n.37454-23A=
ENST00000591111.5:c.34265-23A= ENSP00000465570.1:n.34265-23A=
ENST00000615779.4:c.34522+188A= ENSP00000483597.1:n.34522+188A=
NM_001256850.1:c.34522+188A= NP_001243779.1:n.34522+188A=
NM_001267550.2:c.37454-23A= MANE Select NP_001254479.2:n.37454-23A=
NM_003319.4:c.13283-16500A= NP_003310.4:n.13283-16500A=
NM_133378.4:c.31741+188A= NP_596869.4:n.31741+188A=
NM_133432.3:c.13658-16500A= NP_597676.3:n.13658-16500A=
NM_133437.4:c.13859-16500A= NP_597681.4:n.13859-16500A=
XM_011511729.1:c.36551-23A= XP_011510031.1:n.36551-23A=
XM_011511730.1:c.13469-16500A= XP_011510032.1:n.13469-16500A=
XM_011511731.1:c.13328-16500A= XP_011510033.1:n.13328-16500A=
XM_017004819.1:c.36347-23A= XP_016860308.1:n.36347-23A=
XM_017004820.1:c.31745-23A= XP_016860309.1:n.31745-23A=
XM_017004821.1:c.31742-23A= XP_016860310.1:n.31742-23A=
XM_017004822.1:c.31858+14816A= XP_016860311.1:n.31858+14816A=
XM_017004823.1:c.13424-16500A= XP_016860312.1:n.13424-16500A=
XM_024453094.1:c.33389-23A= XP_024308862.1:n.33389-23A=
XM_024453095.1:c.33386-23A= XP_024308863.1:n.33386-23A=
XM_024453096.1:c.32819-23A= XP_024308864.1:n.32819-23A=
XM_024453097.1:c.31690+14816A= XP_024308865.1:n.31690+14816A=
XM_024453098.1:c.31609+14816A= XP_024308866.1:n.31609+14816A=
XM_024453099.1:c.13424-16500A= XP_024308867.1:n.13424-16500A=
XM_024453100.1:c.203-23A= XP_024308868.1:n.203-23A=