Canonical Allele Identifier: CA1310555850

Gene: TTN

Linked Data

• dbSNP Id: rs2059620169
• gnomAD v4: 2-178630148-TCTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630153_178630156del , CM000664.2:g.178630153_178630156del	GRCh38
NC_000002.11:g.179494880_179494883del , CM000664.1:g.179494880_179494883del	GRCh37
NC_000002.10:g.179203125_179203128del	NCBI36
NG_011618.3:g.205651_205654del , LRG_391:g.205651_205654del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.36577+89_36577+92del	ENSP00000343764.6:n.36577+89_36577+92del
ENST00000342175.11:c.17662+89_17662+92del	ENSP00000340554.6:n.17662+89_17662+92del
ENST00000359218.10:c.17461+89_17461+92del	ENSP00000352154.5:n.17461+89_17461+92del
ENST00000342175.10:c.17662+89_17662+92del	ENSP00000340554.6:n.17662+89_17662+92del
ENST00000342992.10:c.36577+89_36577+92del	ENSP00000343764.6:n.36577+89_36577+92del
ENST00000359218.9:c.17461+89_17461+92del	ENSP00000352154.5:n.17461+89_17461+92del
ENST00000460472.6:c.17086+89_17086+92del	ENSP00000434586.1:n.17086+89_17086+92del
ENST00000589042.5:c.44281+89_44281+92del MANE Select	ENSP00000467141.1:n.44281+89_44281+92del
ENST00000591111.5:c.39358+89_39358+92del	ENSP00000465570.1:n.39358+89_39358+92del
ENST00000615779.4:c.39358+89_39358+92del	ENSP00000483597.1:n.39358+89_39358+92del
NM_001256850.1:c.39358+89_39358+92del	NP_001243779.1:n.39358+89_39358+92del
NM_001267550.2:c.44281+89_44281+92del MANE Select	NP_001254479.2:n.44281+89_44281+92del
NM_003319.4:c.17086+89_17086+92del	NP_003310.4:n.17086+89_17086+92del
NM_133378.4:c.36577+89_36577+92del	NP_596869.4:n.36577+89_36577+92del
NM_133432.3:c.17461+89_17461+92del	NP_597676.3:n.17461+89_17461+92del
NM_133437.4:c.17662+89_17662+92del	NP_597681.4:n.17662+89_17662+92del
XM_011511729.1:c.43378+89_43378+92del	XP_011510031.1:n.43378+89_43378+92del
XM_011511730.1:c.17272+89_17272+92del	XP_011510032.1:n.17272+89_17272+92del
XM_011511731.1:c.17131+89_17131+92del	XP_011510033.1:n.17131+89_17131+92del
XM_017004819.1:c.43174+89_43174+92del	XP_016860308.1:n.43174+89_43174+92del
XM_017004820.1:c.38572+89_38572+92del	XP_016860309.1:n.38572+89_38572+92del
XM_017004821.1:c.38569+89_38569+92del	XP_016860310.1:n.38569+89_38569+92del
XM_017004822.1:c.35611+89_35611+92del	XP_016860311.1:n.35611+89_35611+92del
XM_017004823.1:c.17227+89_17227+92del	XP_016860312.1:n.17227+89_17227+92del
XM_024453094.1:c.38722+89_38722+92del	XP_024308862.1:n.38722+89_38722+92del
XM_024453095.1:c.38719+89_38719+92del	XP_024308863.1:n.38719+89_38719+92del
XM_024453096.1:c.38152+89_38152+92del	XP_024308864.1:n.38152+89_38152+92del
XM_024453097.1:c.35494+89_35494+92del	XP_024308865.1:n.35494+89_35494+92del
XM_024453098.1:c.35413+89_35413+92del	XP_024308866.1:n.35413+89_35413+92del
XM_024453099.1:c.17176+89_17176+92del	XP_024308867.1:n.17176+89_17176+92del
XM_024453100.1:c.7030+89_7030+92del	XP_024308868.1:n.7030+89_7030+92del