Canonical Allele Identifier: CA1310520607

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543268A= , CM000664.2:g.178543268A= GRCh38
NC_000002.11:g.179407995A= , CM000664.1:g.179407995A= GRCh37
NC_000002.10:g.179116241A= NCBI36
NG_011618.3:g.292535T= , LRG_391:g.292535T=
NG_051363.1:g.25442A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.89001T= (TTN) ENSP00000343764.6:p.Thr29667=
ENST00000342175.11:c.70086T= (TTN) ENSP00000340554.6:p.Thr23362=
ENST00000359218.10:c.69885T= (TTN) ENSP00000352154.5:p.Thr23295=
ENST00000342175.10:c.70086T= (TTN) ENSP00000340554.6:p.Thr23362=
ENST00000342992.10:c.89001T= (TTN) ENSP00000343764.6:p.Thr29667=
ENST00000359218.9:c.69885T= (TTN) ENSP00000352154.5:p.Thr23295=
ENST00000460472.6:c.69510T= (TTN) ENSP00000434586.1:p.Thr23170=
ENST00000589042.5:c.96705T= (TTN) MANE Select ENSP00000467141.1:p.Thr32235=
ENST00000591111.5:c.91782T= (TTN) ENSP00000465570.1:p.Thr30594=
ENST00000615779.4:c.91782T= (TTN) ENSP00000483597.1:p.Thr30594=
NM_001256850.1:c.91782T= (TTN) NP_001243779.1:p.Thr30594=
NM_001267550.2:c.96705T= (TTN) MANE Select NP_001254479.2:p.Thr32235=
NM_003319.4:c.69510T= (TTN) NP_003310.4:p.Thr23170=
NM_133378.4:c.89001T= (TTN) NP_596869.4:p.Thr29667=
NM_133432.3:c.69885T= (TTN) NP_597676.3:p.Thr23295=
NM_133437.4:c.70086T= (TTN) NP_597681.4:p.Thr23362=
NR_038271.1:n.446+19632A= (TTN-AS1)
NR_038272.1:n.2043+907A= (TTN-AS1)
XM_011511729.1:c.95802T= (TTN) XP_011510031.1:p.Thr31934=
XM_011511730.1:c.69696T= (TTN) XP_011510032.1:p.Thr23232=
XM_011511731.1:c.69555T= (TTN) XP_011510033.1:p.Thr23185=
XM_017004819.1:c.95598T= (TTN) XP_016860308.1:p.Thr31866=
XM_017004820.1:c.90996T= (TTN) XP_016860309.1:p.Thr30332=
XM_017004821.1:c.90993T= (TTN) XP_016860310.1:p.Thr30331=
XM_017004822.1:c.88035T= (TTN) XP_016860311.1:p.Thr29345=
XM_017004823.1:c.69651T= (TTN) XP_016860312.1:p.Thr23217=
XM_024453094.1:c.91146T= (TTN) XP_024308862.1:p.Thr30382=
XM_024453095.1:c.91143T= (TTN) XP_024308863.1:p.Thr30381=
XM_024453096.1:c.90576T= (TTN) XP_024308864.1:p.Thr30192=
XM_024453097.1:c.87918T= (TTN) XP_024308865.1:p.Thr29306=
XM_024453098.1:c.87837T= (TTN) XP_024308866.1:p.Thr29279=
XM_024453099.1:c.69600T= (TTN) XP_024308867.1:p.Thr23200=
XM_024453100.1:c.59454T= (TTN) XP_024308868.1:p.Thr19818=