Canonical Allele Identifier: CA1310532912

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178574794T= , CM000664.2:g.178574794T= GRCh38
NC_000002.11:g.179439521T= , CM000664.1:g.179439521T= GRCh37
NC_000002.10:g.179147767T= NCBI36
NG_011618.3:g.261009A= , LRG_391:g.261009A=
NG_051363.1:g.56968T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.63634A= (TTN) ENSP00000343764.6:p.Thr21212=
ENST00000342175.11:c.44719A= (TTN) ENSP00000340554.6:p.Thr14907=
ENST00000359218.10:c.44518A= (TTN) ENSP00000352154.5:p.Thr14840=
ENST00000342175.10:c.44719A= (TTN) ENSP00000340554.6:p.Thr14907=
ENST00000342992.10:c.63634A= (TTN) ENSP00000343764.6:p.Thr21212=
ENST00000359218.9:c.44518A= (TTN) ENSP00000352154.5:p.Thr14840=
ENST00000460472.6:c.44143A= (TTN) ENSP00000434586.1:p.Thr14715=
ENST00000589042.5:c.71338A= (TTN) MANE Select ENSP00000467141.1:p.Thr23780=
ENST00000591111.5:c.66415A= (TTN) ENSP00000465570.1:p.Thr22139=
ENST00000615779.4:c.66415A= (TTN) ENSP00000483597.1:p.Thr22139=
NM_001256850.1:c.66415A= (TTN) NP_001243779.1:p.Thr22139=
NM_001267550.2:c.71338A= (TTN) MANE Select NP_001254479.2:p.Thr23780=
NM_003319.4:c.44143A= (TTN) NP_003310.4:p.Thr14715=
NM_133378.4:c.63634A= (TTN) NP_596869.4:p.Thr21212=
NM_133432.3:c.44518A= (TTN) NP_597676.3:p.Thr14840=
NM_133437.4:c.44719A= (TTN) NP_597681.4:p.Thr14907=
NR_038271.1:n.596+3345T= (TTN-AS1)
NR_038272.1:n.2044-7778T= (TTN-AS1)
XM_011511729.1:c.70435A= (TTN) XP_011510031.1:p.Thr23479=
XM_011511730.1:c.44329A= (TTN) XP_011510032.1:p.Thr14777=
XM_011511731.1:c.44188A= (TTN) XP_011510033.1:p.Thr14730=
XM_017004819.1:c.70231A= (TTN) XP_016860308.1:p.Thr23411=
XM_017004820.1:c.65629A= (TTN) XP_016860309.1:p.Thr21877=
XM_017004821.1:c.65626A= (TTN) XP_016860310.1:p.Thr21876=
XM_017004822.1:c.62668A= (TTN) XP_016860311.1:p.Thr20890=
XM_017004823.1:c.44284A= (TTN) XP_016860312.1:p.Thr14762=
XM_024453094.1:c.65779A= (TTN) XP_024308862.1:p.Thr21927=
XM_024453095.1:c.65776A= (TTN) XP_024308863.1:p.Thr21926=
XM_024453096.1:c.65209A= (TTN) XP_024308864.1:p.Thr21737=
XM_024453097.1:c.62551A= (TTN) XP_024308865.1:p.Thr20851=
XM_024453098.1:c.62470A= (TTN) XP_024308866.1:p.Thr20824=
XM_024453099.1:c.44233A= (TTN) XP_024308867.1:p.Thr14745=
XM_024453100.1:c.34087A= (TTN) XP_024308868.1:p.Thr11363=