Canonical Allele Identifier: CA2753331329

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178544118_178544202del , CM000664.2:g.178544118_178544202del GRCh38
NC_000002.11:g.179408845_179408929del , CM000664.1:g.179408845_179408929del GRCh37
NC_000002.10:g.179117091_179117175del NCBI36
NG_011618.3:g.291603_291687del , LRG_391:g.291603_291687del
NG_051363.1:g.26292_26376del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.88324+1_88325-1del (TTN)
ENST00000342175.11:c.69409+1_69410-1del (TTN)
ENST00000359218.10:c.69208+1_69209-1del (TTN)
ENST00000342175.10:c.69409+1_69410-1del (TTN)
ENST00000342992.10:c.88324+1_88325-1del (TTN)
ENST00000359218.9:c.69208+1_69209-1del (TTN)
ENST00000460472.6:c.68833+1_68834-1del (TTN)
ENST00000589042.5:c.96028+1_96029-1del (TTN)
ENST00000591111.5:c.91105+1_91106-1del (TTN)
ENST00000615779.4:c.91105+1_91106-1del (TTN)
NM_001256850.1:c.91105+1_91106-1del (TTN)
NM_001267550.2:c.96028+1_96029-1del (TTN)
NM_003319.4:c.68833+1_68834-1del (TTN)
NM_133378.4:c.88324+1_88325-1del (TTN)
NM_133432.3:c.69208+1_69209-1del (TTN)
NM_133437.4:c.69409+1_69410-1del (TTN)
NR_038271.1:n.446+20482_446+20566del (TTN-AS1)
NR_038272.1:n.2043+1757_2043+1841del (TTN-AS1)
XM_011511729.1:c.95125+1_95126-1del (TTN)
XM_011511730.1:c.69019+1_69020-1del (TTN)
XM_011511731.1:c.68878+1_68879-1del (TTN)
XM_017004819.1:c.94921+1_94922-1del (TTN)
XM_017004820.1:c.90319+1_90320-1del (TTN)
XM_017004821.1:c.90316+1_90317-1del (TTN)
XM_017004822.1:c.87358+1_87359-1del (TTN)
XM_017004823.1:c.68974+1_68975-1del (TTN)
XM_024453094.1:c.90469+1_90470-1del (TTN)
XM_024453095.1:c.90466+1_90467-1del (TTN)
XM_024453096.1:c.89899+1_89900-1del (TTN)
XM_024453097.1:c.87241+1_87242-1del (TTN)
XM_024453098.1:c.87160+1_87161-1del (TTN)
XM_024453099.1:c.68923+1_68924-1del (TTN)
XM_024453100.1:c.58777+1_58778-1del (TTN)