Canonical Allele Identifier: CA1310511453

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530079T= , CM000664.2:g.178530079T= GRCh38
NC_000002.11:g.179394806T= , CM000664.1:g.179394806T= GRCh37
NC_000002.10:g.179103052T= NCBI36
NG_011618.3:g.305724A= , LRG_391:g.305724A=
NG_051363.1:g.12253T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98708A= (TTN) ENSP00000343764.6:p.Asp32903=
ENST00000342175.11:c.79793A= (TTN) ENSP00000340554.6:p.Asp26598=
ENST00000359218.10:c.79592A= (TTN) ENSP00000352154.5:p.Asp26531=
ENST00000342175.10:c.79793A= (TTN) ENSP00000340554.6:p.Asp26598=
ENST00000342992.10:c.98708A= (TTN) ENSP00000343764.6:p.Asp32903=
ENST00000359218.9:c.79592A= (TTN) ENSP00000352154.5:p.Asp26531=
ENST00000460472.6:c.79217A= (TTN) ENSP00000434586.1:p.Asp26406=
ENST00000589042.5:c.106412A= (TTN) MANE Select ENSP00000467141.1:p.Asp35471=
ENST00000591111.5:c.101489A= (TTN) ENSP00000465570.1:p.Asp33830=
ENST00000615779.4:c.101489A= (TTN) ENSP00000483597.1:p.Asp33830=
NM_001256850.1:c.101489A= (TTN) NP_001243779.1:p.Asp33830=
NM_001267550.2:c.106412A= (TTN) MANE Select NP_001254479.2:p.Asp35471=
NM_003319.4:c.79217A= (TTN) NP_003310.4:p.Asp26406=
NM_133378.4:c.98708A= (TTN) NP_596869.4:p.Asp32903=
NM_133432.3:c.79592A= (TTN) NP_597676.3:p.Asp26531=
NM_133437.4:c.79793A= (TTN) NP_597681.4:p.Asp26598=
NR_038271.1:n.446+6443T= (TTN-AS1)
NR_038272.1:n.220-5653T= (TTN-AS1)
XM_011511729.1:c.105509A= (TTN) XP_011510031.1:p.Asp35170=
XM_011511730.1:c.79403A= (TTN) XP_011510032.1:p.Asp26468=
XM_011511731.1:c.79262A= (TTN) XP_011510033.1:p.Asp26421=
XM_017004819.1:c.105305A= (TTN) XP_016860308.1:p.Asp35102=
XM_017004820.1:c.100703A= (TTN) XP_016860309.1:p.Asp33568=
XM_017004821.1:c.100700A= (TTN) XP_016860310.1:p.Asp33567=
XM_017004822.1:c.97742A= (TTN) XP_016860311.1:p.Asp32581=
XM_017004823.1:c.79358A= (TTN) XP_016860312.1:p.Asp26453=
XM_024453094.1:c.100853A= (TTN) XP_024308862.1:p.Asp33618=
XM_024453095.1:c.100850A= (TTN) XP_024308863.1:p.Asp33617=
XM_024453096.1:c.100283A= (TTN) XP_024308864.1:p.Asp33428=
XM_024453097.1:c.97625A= (TTN) XP_024308865.1:p.Asp32542=
XM_024453098.1:c.97544A= (TTN) XP_024308866.1:p.Asp32515=
XM_024453099.1:c.79307A= (TTN) XP_024308867.1:p.Asp26436=
XM_024453100.1:c.69161A= (TTN) XP_024308868.1:p.Asp23054=