Canonical Allele Identifier: CA1039714115

Gene: TTN

Linked Data

• dbSNP Id: rs2059629579
• gnomAD v3: 2-178630213-AT-A
• gnomAD v4: 2-178630213-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630216del , CM000664.2:g.178630216del	GRCh38
NC_000002.11:g.179494943del , CM000664.1:g.179494943del	GRCh37
NC_000002.10:g.179203188del	NCBI36
NG_011618.3:g.205589del , LRG_391:g.205589del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36577+27del	ENSP00000343764.6:n.36577+27del
ENST00000342175.11:c.17662+27del	ENSP00000340554.6:n.17662+27del
ENST00000359218.10:c.17461+27del	ENSP00000352154.5:n.17461+27del
ENST00000342175.10:c.17662+27del	ENSP00000340554.6:n.17662+27del
ENST00000342992.10:c.36577+27del	ENSP00000343764.6:n.36577+27del
ENST00000359218.9:c.17461+27del	ENSP00000352154.5:n.17461+27del
ENST00000460472.6:c.17086+27del	ENSP00000434586.1:n.17086+27del
ENST00000589042.5:c.44281+27del MANE Select	ENSP00000467141.1:n.44281+27del
ENST00000591111.5:c.39358+27del	ENSP00000465570.1:n.39358+27del
ENST00000615779.4:c.39358+27del	ENSP00000483597.1:n.39358+27del
NM_001256850.1:c.39358+27del	NP_001243779.1:n.39358+27del
NM_001267550.2:c.44281+27del MANE Select	NP_001254479.2:n.44281+27del
NM_003319.4:c.17086+27del	NP_003310.4:n.17086+27del
NM_133378.4:c.36577+27del	NP_596869.4:n.36577+27del
NM_133432.3:c.17461+27del	NP_597676.3:n.17461+27del
NM_133437.4:c.17662+27del	NP_597681.4:n.17662+27del
XM_011511729.1:c.43378+27del	XP_011510031.1:n.43378+27del
XM_011511730.1:c.17272+27del	XP_011510032.1:n.17272+27del
XM_011511731.1:c.17131+27del	XP_011510033.1:n.17131+27del
XM_017004819.1:c.43174+27del	XP_016860308.1:n.43174+27del
XM_017004820.1:c.38572+27del	XP_016860309.1:n.38572+27del
XM_017004821.1:c.38569+27del	XP_016860310.1:n.38569+27del
XM_017004822.1:c.35611+27del	XP_016860311.1:n.35611+27del
XM_017004823.1:c.17227+27del	XP_016860312.1:n.17227+27del
XM_024453094.1:c.38722+27del	XP_024308862.1:n.38722+27del
XM_024453095.1:c.38719+27del	XP_024308863.1:n.38719+27del
XM_024453096.1:c.38152+27del	XP_024308864.1:n.38152+27del
XM_024453097.1:c.35494+27del	XP_024308865.1:n.35494+27del
XM_024453098.1:c.35413+27del	XP_024308866.1:n.35413+27del
XM_024453099.1:c.17176+27del	XP_024308867.1:n.17176+27del
XM_024453100.1:c.7030+27del	XP_024308868.1:n.7030+27del