Canonical Allele Identifier: CA2586970783

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630228_178630243del , CM000664.2:g.178630228_178630243del	GRCh38
NC_000002.11:g.179494955_179494970del , CM000664.1:g.179494955_179494970del	GRCh37
NC_000002.10:g.179203200_179203215del	NCBI36
NG_011618.3:g.205561_205576del , LRG_391:g.205561_205576del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36576_36577+14del
ENST00000342175.11:c.17661_17662+14del
ENST00000359218.10:c.17460_17461+14del
ENST00000342175.10:c.17661_17662+14del
ENST00000342992.10:c.36576_36577+14del
ENST00000359218.9:c.17460_17461+14del
ENST00000460472.6:c.17085_17086+14del
ENST00000589042.5:c.44280_44281+14del
ENST00000591111.5:c.39357_39358+14del
ENST00000615779.4:c.39357_39358+14del
NM_001256850.1:c.39357_39358+14del
NM_001267550.2:c.44280_44281+14del
NM_003319.4:c.17085_17086+14del
NM_133378.4:c.36576_36577+14del
NM_133432.3:c.17460_17461+14del
NM_133437.4:c.17661_17662+14del
XM_011511729.1:c.43377_43378+14del
XM_011511730.1:c.17271_17272+14del
XM_011511731.1:c.17130_17131+14del
XM_017004819.1:c.43173_43174+14del
XM_017004820.1:c.38571_38572+14del
XM_017004821.1:c.38568_38569+14del
XM_017004822.1:c.35610_35611+14del
XM_017004823.1:c.17226_17227+14del
XM_024453094.1:c.38721_38722+14del
XM_024453095.1:c.38718_38719+14del
XM_024453096.1:c.38151_38152+14del
XM_024453097.1:c.35493_35494+14del
XM_024453098.1:c.35412_35413+14del
XM_024453099.1:c.17175_17176+14del
XM_024453100.1:c.7029_7030+14del