Canonical Allele Identifier: CA2753331052

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178539968_178540068del , CM000664.2:g.178539968_178540068del GRCh38
NC_000002.11:g.179404695_179404795del , CM000664.1:g.179404695_179404795del GRCh37
NC_000002.10:g.179112941_179113041del NCBI36
NG_011618.3:g.295736_295836del , LRG_391:g.295736_295836del
NG_051363.1:g.22142_22242del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.90394+1_90395-1del (TTN)
ENST00000342175.11:c.71479+1_71480-1del (TTN)
ENST00000359218.10:c.71278+1_71279-1del (TTN)
ENST00000342175.10:c.71479+1_71480-1del (TTN)
ENST00000342992.10:c.90394+1_90395-1del (TTN)
ENST00000359218.9:c.71278+1_71279-1del (TTN)
ENST00000460472.6:c.70903+1_70904-1del (TTN)
ENST00000589042.5:c.98098+1_98099-1del (TTN)
ENST00000591111.5:c.93175+1_93176-1del (TTN)
ENST00000615779.4:c.93175+1_93176-1del (TTN)
NM_001256850.1:c.93175+1_93176-1del (TTN)
NM_001267550.2:c.98098+1_98099-1del (TTN)
NM_003319.4:c.70903+1_70904-1del (TTN)
NM_133378.4:c.90394+1_90395-1del (TTN)
NM_133432.3:c.71278+1_71279-1del (TTN)
NM_133437.4:c.71479+1_71480-1del (TTN)
NR_038271.1:n.446+16332_446+16432del (TTN-AS1)
NR_038272.1:n.1840+78_1841-39del (TTN-AS1)
XM_011511729.1:c.97195+1_97196-1del (TTN)
XM_011511730.1:c.71089+1_71090-1del (TTN)
XM_011511731.1:c.70948+1_70949-1del (TTN)
XM_017004819.1:c.96991+1_96992-1del (TTN)
XM_017004820.1:c.92389+1_92390-1del (TTN)
XM_017004821.1:c.92386+1_92387-1del (TTN)
XM_017004822.1:c.89428+1_89429-1del (TTN)
XM_017004823.1:c.71044+1_71045-1del (TTN)
XM_024453094.1:c.92539+1_92540-1del (TTN)
XM_024453095.1:c.92536+1_92537-1del (TTN)
XM_024453096.1:c.91969+1_91970-1del (TTN)
XM_024453097.1:c.89311+1_89312-1del (TTN)
XM_024453098.1:c.89230+1_89231-1del (TTN)
XM_024453099.1:c.70993+1_70994-1del (TTN)
XM_024453100.1:c.60847+1_60848-1del (TTN)