Canonical Allele Identifier: CA1310521154

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178543892T= , CM000664.2:g.178543892T= GRCh38
NC_000002.11:g.179408619T= , CM000664.1:g.179408619T= GRCh37
NC_000002.10:g.179116865T= NCBI36
NG_011618.3:g.291911A= , LRG_391:g.291911A=
NG_051363.1:g.26066T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.88548A= (TTN) ENSP00000343764.6:p.Thr29516=
ENST00000342175.11:c.69633A= (TTN) ENSP00000340554.6:p.Thr23211=
ENST00000359218.10:c.69432A= (TTN) ENSP00000352154.5:p.Thr23144=
ENST00000342175.10:c.69633A= (TTN) ENSP00000340554.6:p.Thr23211=
ENST00000342992.10:c.88548A= (TTN) ENSP00000343764.6:p.Thr29516=
ENST00000359218.9:c.69432A= (TTN) ENSP00000352154.5:p.Thr23144=
ENST00000460472.6:c.69057A= (TTN) ENSP00000434586.1:p.Thr23019=
ENST00000589042.5:c.96252A= (TTN) MANE Select ENSP00000467141.1:p.Thr32084=
ENST00000591111.5:c.91329A= (TTN) ENSP00000465570.1:p.Thr30443=
ENST00000615779.4:c.91329A= (TTN) ENSP00000483597.1:p.Thr30443=
NM_001256850.1:c.91329A= (TTN) NP_001243779.1:p.Thr30443=
NM_001267550.2:c.96252A= (TTN) MANE Select NP_001254479.2:p.Thr32084=
NM_003319.4:c.69057A= (TTN) NP_003310.4:p.Thr23019=
NM_133378.4:c.88548A= (TTN) NP_596869.4:p.Thr29516=
NM_133432.3:c.69432A= (TTN) NP_597676.3:p.Thr23144=
NM_133437.4:c.69633A= (TTN) NP_597681.4:p.Thr23211=
NR_038271.1:n.446+20256T= (TTN-AS1)
NR_038272.1:n.2043+1531T= (TTN-AS1)
XM_011511729.1:c.95349A= (TTN) XP_011510031.1:p.Thr31783=
XM_011511730.1:c.69243A= (TTN) XP_011510032.1:p.Thr23081=
XM_011511731.1:c.69102A= (TTN) XP_011510033.1:p.Thr23034=
XM_017004819.1:c.95145A= (TTN) XP_016860308.1:p.Thr31715=
XM_017004820.1:c.90543A= (TTN) XP_016860309.1:p.Thr30181=
XM_017004821.1:c.90540A= (TTN) XP_016860310.1:p.Thr30180=
XM_017004822.1:c.87582A= (TTN) XP_016860311.1:p.Thr29194=
XM_017004823.1:c.69198A= (TTN) XP_016860312.1:p.Thr23066=
XM_024453094.1:c.90693A= (TTN) XP_024308862.1:p.Thr30231=
XM_024453095.1:c.90690A= (TTN) XP_024308863.1:p.Thr30230=
XM_024453096.1:c.90123A= (TTN) XP_024308864.1:p.Thr30041=
XM_024453097.1:c.87465A= (TTN) XP_024308865.1:p.Thr29155=
XM_024453098.1:c.87384A= (TTN) XP_024308866.1:p.Thr29128=
XM_024453099.1:c.69147A= (TTN) XP_024308867.1:p.Thr23049=
XM_024453100.1:c.59001A= (TTN) XP_024308868.1:p.Thr19667=