Canonical Allele Identifier: CA538435061

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1202788527
• gnomAD v2: 2-179404691-ATTCTGG-A
• gnomAD v4: 2-178539964-ATTCTGG-A
• MyVariant Identifiers: chr2:g.179404692_179404697del (hg19) ; chr2:g.178539965_178539970del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178539965_178539970del , CM000664.2:g.178539965_178539970del	GRCh38
NC_000002.11:g.179404692_179404697del , CM000664.1:g.179404692_179404697del	GRCh37
NC_000002.10:g.179112938_179112943del	NCBI36
NG_011618.3:g.295833_295838del , LRG_391:g.295833_295838del
NG_051363.1:g.22139_22144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.90395-4_90396del (TTN)
ENST00000342175.11:c.71480-4_71481del (TTN)
ENST00000359218.10:c.71279-4_71280del (TTN)
ENST00000342175.10:c.71480-4_71481del (TTN)
ENST00000342992.10:c.90395-4_90396del (TTN)
ENST00000359218.9:c.71279-4_71280del (TTN)
ENST00000460472.6:c.70904-4_70905del (TTN)
ENST00000589042.5:c.98099-4_98100del (TTN)
ENST00000591111.5:c.93176-4_93177del (TTN)
ENST00000615779.4:c.93176-4_93177del (TTN)
NM_001256850.1:c.93176-4_93177del (TTN)
NM_001267550.2:c.98099-4_98100del (TTN)
NM_003319.4:c.70904-4_70905del (TTN)
NM_133378.4:c.90395-4_90396del (TTN)
NM_133432.3:c.71279-4_71280del (TTN)
NM_133437.4:c.71480-4_71481del (TTN)
NR_038271.1:n.446+16329_446+16334del (TTN-AS1)
NR_038272.1:n.1840+75_1840+80del (TTN-AS1)
XM_011511729.1:c.97196-4_97197del (TTN)
XM_011511730.1:c.71090-4_71091del (TTN)
XM_011511731.1:c.70949-4_70950del (TTN)
XM_017004819.1:c.96992-4_96993del (TTN)
XM_017004820.1:c.92390-4_92391del (TTN)
XM_017004821.1:c.92387-4_92388del (TTN)
XM_017004822.1:c.89429-4_89430del (TTN)
XM_017004823.1:c.71045-4_71046del (TTN)
XM_024453094.1:c.92540-4_92541del (TTN)
XM_024453095.1:c.92537-4_92538del (TTN)
XM_024453096.1:c.91970-4_91971del (TTN)
XM_024453097.1:c.89312-4_89313del (TTN)
XM_024453098.1:c.89231-4_89232del (TTN)
XM_024453099.1:c.70994-4_70995del (TTN)
XM_024453100.1:c.60848-4_60849del (TTN)