Canonical Allele Identifier: CA1310515187

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178537066A= , CM000664.2:g.178537066A= GRCh38
NC_000002.11:g.179401793A= , CM000664.1:g.179401793A= GRCh37
NC_000002.10:g.179110039A= NCBI36
NG_011618.3:g.298737T= , LRG_391:g.298737T=
NG_051363.1:g.19240A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.92339T= (TTN) ENSP00000343764.6:p.Val30780=
ENST00000342175.11:c.73424T= (TTN) ENSP00000340554.6:p.Val24475=
ENST00000359218.10:c.73223T= (TTN) ENSP00000352154.5:p.Val24408=
ENST00000342175.10:c.73424T= (TTN) ENSP00000340554.6:p.Val24475=
ENST00000342992.10:c.92339T= (TTN) ENSP00000343764.6:p.Val30780=
ENST00000359218.9:c.73223T= (TTN) ENSP00000352154.5:p.Val24408=
ENST00000460472.6:c.72848T= (TTN) ENSP00000434586.1:p.Val24283=
ENST00000589042.5:c.100043T= (TTN) MANE Select ENSP00000467141.1:p.Val33348=
ENST00000591111.5:c.95120T= (TTN) ENSP00000465570.1:p.Val31707=
ENST00000615779.4:c.95120T= (TTN) ENSP00000483597.1:p.Val31707=
NM_001256850.1:c.95120T= (TTN) NP_001243779.1:p.Val31707=
NM_001267550.2:c.100043T= (TTN) MANE Select NP_001254479.2:p.Val33348=
NM_003319.4:c.72848T= (TTN) NP_003310.4:p.Val24283=
NM_133378.4:c.92339T= (TTN) NP_596869.4:p.Val30780=
NM_133432.3:c.73223T= (TTN) NP_597676.3:p.Val24408=
NM_133437.4:c.73424T= (TTN) NP_597681.4:p.Val24475=
NR_038271.1:n.446+13430A= (TTN-AS1)
NR_038272.1:n.317-295A= (TTN-AS1)
XM_011511729.1:c.99140T= (TTN) XP_011510031.1:p.Val33047=
XM_011511730.1:c.73034T= (TTN) XP_011510032.1:p.Val24345=
XM_011511731.1:c.72893T= (TTN) XP_011510033.1:p.Val24298=
XM_017004819.1:c.98936T= (TTN) XP_016860308.1:p.Val32979=
XM_017004820.1:c.94334T= (TTN) XP_016860309.1:p.Val31445=
XM_017004821.1:c.94331T= (TTN) XP_016860310.1:p.Val31444=
XM_017004822.1:c.91373T= (TTN) XP_016860311.1:p.Val30458=
XM_017004823.1:c.72989T= (TTN) XP_016860312.1:p.Val24330=
XM_024453094.1:c.94484T= (TTN) XP_024308862.1:p.Val31495=
XM_024453095.1:c.94481T= (TTN) XP_024308863.1:p.Val31494=
XM_024453096.1:c.93914T= (TTN) XP_024308864.1:p.Val31305=
XM_024453097.1:c.91256T= (TTN) XP_024308865.1:p.Val30419=
XM_024453098.1:c.91175T= (TTN) XP_024308866.1:p.Val30392=
XM_024453099.1:c.72938T= (TTN) XP_024308867.1:p.Val24313=
XM_024453100.1:c.62792T= (TTN) XP_024308868.1:p.Val20931=