Canonical Allele Identifier: CA1310539673

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178590936A= , CM000664.2:g.178590936A= GRCh38
NC_000002.11:g.179455663A= , CM000664.1:g.179455663A= GRCh37
NC_000002.10:g.179163909A= NCBI36
NG_011618.3:g.244867T= , LRG_391:g.244867T=
NG_051363.1:g.73110A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.53085T= (TTN) ENSP00000343764.6:p.Thr17695=
ENST00000342175.11:c.34170T= (TTN) ENSP00000340554.6:p.Thr11390=
ENST00000359218.10:c.33969T= (TTN) ENSP00000352154.5:p.Thr11323=
ENST00000342175.10:c.34170T= (TTN) ENSP00000340554.6:p.Thr11390=
ENST00000342992.10:c.53085T= (TTN) ENSP00000343764.6:p.Thr17695=
ENST00000359218.9:c.33969T= (TTN) ENSP00000352154.5:p.Thr11323=
ENST00000460472.6:c.33594T= (TTN) ENSP00000434586.1:p.Thr11198=
ENST00000589042.5:c.60789T= (TTN) MANE Select ENSP00000467141.1:p.Thr20263=
ENST00000591111.5:c.55866T= (TTN) ENSP00000465570.1:p.Thr18622=
ENST00000615779.4:c.55866T= (TTN) ENSP00000483597.1:p.Thr18622=
NM_001256850.1:c.55866T= (TTN) NP_001243779.1:p.Thr18622=
NM_001267550.2:c.60789T= (TTN) MANE Select NP_001254479.2:p.Thr20263=
NM_003319.4:c.33594T= (TTN) NP_003310.4:p.Thr11198=
NM_133378.4:c.53085T= (TTN) NP_596869.4:p.Thr17695=
NM_133432.3:c.33969T= (TTN) NP_597676.3:p.Thr11323=
NM_133437.4:c.34170T= (TTN) NP_597681.4:p.Thr11390=
NR_038271.1:n.597-6660A= (TTN-AS1)
NR_038272.1:n.3189-203A= (TTN-AS1)
XM_011511729.1:c.59886T= (TTN) XP_011510031.1:p.Thr19962=
XM_011511730.1:c.33780T= (TTN) XP_011510032.1:p.Thr11260=
XM_011511731.1:c.33639T= (TTN) XP_011510033.1:p.Thr11213=
XM_017004819.1:c.59682T= (TTN) XP_016860308.1:p.Thr19894=
XM_017004820.1:c.55080T= (TTN) XP_016860309.1:p.Thr18360=
XM_017004821.1:c.55077T= (TTN) XP_016860310.1:p.Thr18359=
XM_017004822.1:c.52119T= (TTN) XP_016860311.1:p.Thr17373=
XM_017004823.1:c.33735T= (TTN) XP_016860312.1:p.Thr11245=
XM_024453094.1:c.55230T= (TTN) XP_024308862.1:p.Thr18410=
XM_024453095.1:c.55227T= (TTN) XP_024308863.1:p.Thr18409=
XM_024453096.1:c.54660T= (TTN) XP_024308864.1:p.Thr18220=
XM_024453097.1:c.52002T= (TTN) XP_024308865.1:p.Thr17334=
XM_024453098.1:c.51921T= (TTN) XP_024308866.1:p.Thr17307=
XM_024453099.1:c.33684T= (TTN) XP_024308867.1:p.Thr11228=
XM_024453100.1:c.23538T= (TTN) XP_024308868.1:p.Thr7846=