Canonical Allele Identifier: CA1998706

Gene: TTN

Linked Data

• dbSNP Id: rs766171557
• ExAC: 2:179553395 AT / A
• gnomAD v2: 2-179553395-AT-A
• gnomAD v4: 2-178688668-AT-A
• MyVariant Identifiers: chr2:g.179553396del (hg19) ; chr2:g.178688669del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178688670del , CM000664.2:g.178688670del	GRCh38
NC_000002.11:g.179553397del , CM000664.1:g.179553397del	GRCh37
NC_000002.10:g.179261642del	NCBI36
NG_011618.3:g.147134del , LRG_391:g.147134del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.28465+8del	ENSP00000343764.6:n.28465+8del
ENST00000342175.11:c.13859-46352del	ENSP00000340554.6:n.13859-46352del
ENST00000359218.10:c.13658-46352del	ENSP00000352154.5:n.13658-46352del
ENST00000342175.10:c.13859-46352del	ENSP00000340554.6:n.13859-46352del
ENST00000342992.10:c.28465+8del	ENSP00000343764.6:n.28465+8del
ENST00000359218.9:c.13658-46352del	ENSP00000352154.5:n.13658-46352del
ENST00000414766.5:c.1729+384del	ENSP00000401501.1:n.1729+384del
ENST00000460472.6:c.13283-46352del	ENSP00000434586.1:n.13283-46352del
ENST00000589042.5:c.32197+8del MANE Select	ENSP00000467141.1:n.32197+8del
ENST00000591111.5:c.31246+8del	ENSP00000465570.1:n.31246+8del
ENST00000615779.4:c.31246+8del	ENSP00000483597.1:n.31246+8del
NM_001256850.1:c.31246+8del	NP_001243779.1:n.31246+8del
NM_001267550.2:c.32197+8del MANE Select	NP_001254479.2:n.32197+8del
NM_003319.4:c.13283-46352del	NP_003310.4:n.13283-46352del
NM_133378.4:c.28465+8del	NP_596869.4:n.28465+8del
NM_133432.3:c.13658-46352del	NP_597676.3:n.13658-46352del
NM_133437.4:c.13859-46352del	NP_597681.4:n.13859-46352del
XM_011511729.1:c.31294+8del	XP_011510031.1:n.31294+8del
XM_011511730.1:c.13469-46352del	XP_011510032.1:n.13469-46352del
XM_011511731.1:c.13328-46352del	XP_011510033.1:n.13328-46352del
XM_017004819.1:c.31249+8del	XP_016860308.1:n.31249+8del
XM_017004820.1:c.28468+8del	XP_016860309.1:n.28468+8del
XM_017004821.1:c.28465+8del	XP_016860310.1:n.28465+8del
XM_017004822.1:c.31147+384del	XP_016860311.1:n.31147+384del
XM_017004823.1:c.13424-46352del	XP_016860312.1:n.13424-46352del
XM_024453094.1:c.31249+8del	XP_024308862.1:n.31249+8del
XM_024453095.1:c.31249+8del	XP_024308863.1:n.31249+8del
XM_024453096.1:c.31249+8del	XP_024308864.1:n.31249+8del
XM_024453097.1:c.30898+1144del	XP_024308865.1:n.30898+1144del
XM_024453098.1:c.30898+1144del	XP_024308866.1:n.30898+1144del
XM_024453099.1:c.13424-46352del	XP_024308867.1:n.13424-46352del