Canonical Allele Identifier: CA1310511413

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530068A= , CM000664.2:g.178530068A= GRCh38
NC_000002.11:g.179394795A= , CM000664.1:g.179394795A= GRCh37
NC_000002.10:g.179103041A= NCBI36
NG_011618.3:g.305735T= , LRG_391:g.305735T=
NG_051363.1:g.12242A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98719T= (TTN) ENSP00000343764.6:p.Phe32907=
ENST00000342175.11:c.79804T= (TTN) ENSP00000340554.6:p.Phe26602=
ENST00000359218.10:c.79603T= (TTN) ENSP00000352154.5:p.Phe26535=
ENST00000342175.10:c.79804T= (TTN) ENSP00000340554.6:p.Phe26602=
ENST00000342992.10:c.98719T= (TTN) ENSP00000343764.6:p.Phe32907=
ENST00000359218.9:c.79603T= (TTN) ENSP00000352154.5:p.Phe26535=
ENST00000460472.6:c.79228T= (TTN) ENSP00000434586.1:p.Phe26410=
ENST00000589042.5:c.106423T= (TTN) MANE Select ENSP00000467141.1:p.Phe35475=
ENST00000591111.5:c.101500T= (TTN) ENSP00000465570.1:p.Phe33834=
ENST00000615779.4:c.101500T= (TTN) ENSP00000483597.1:p.Phe33834=
NM_001256850.1:c.101500T= (TTN) NP_001243779.1:p.Phe33834=
NM_001267550.2:c.106423T= (TTN) MANE Select NP_001254479.2:p.Phe35475=
NM_003319.4:c.79228T= (TTN) NP_003310.4:p.Phe26410=
NM_133378.4:c.98719T= (TTN) NP_596869.4:p.Phe32907=
NM_133432.3:c.79603T= (TTN) NP_597676.3:p.Phe26535=
NM_133437.4:c.79804T= (TTN) NP_597681.4:p.Phe26602=
NR_038271.1:n.446+6432A= (TTN-AS1)
NR_038272.1:n.220-5664A= (TTN-AS1)
XM_011511729.1:c.105520T= (TTN) XP_011510031.1:p.Phe35174=
XM_011511730.1:c.79414T= (TTN) XP_011510032.1:p.Phe26472=
XM_011511731.1:c.79273T= (TTN) XP_011510033.1:p.Phe26425=
XM_017004819.1:c.105316T= (TTN) XP_016860308.1:p.Phe35106=
XM_017004820.1:c.100714T= (TTN) XP_016860309.1:p.Phe33572=
XM_017004821.1:c.100711T= (TTN) XP_016860310.1:p.Phe33571=
XM_017004822.1:c.97753T= (TTN) XP_016860311.1:p.Phe32585=
XM_017004823.1:c.79369T= (TTN) XP_016860312.1:p.Phe26457=
XM_024453094.1:c.100864T= (TTN) XP_024308862.1:p.Phe33622=
XM_024453095.1:c.100861T= (TTN) XP_024308863.1:p.Phe33621=
XM_024453096.1:c.100294T= (TTN) XP_024308864.1:p.Phe33432=
XM_024453097.1:c.97636T= (TTN) XP_024308865.1:p.Phe32546=
XM_024453098.1:c.97555T= (TTN) XP_024308866.1:p.Phe32519=
XM_024453099.1:c.79318T= (TTN) XP_024308867.1:p.Phe26440=
XM_024453100.1:c.69172T= (TTN) XP_024308868.1:p.Phe23058=