Canonical Allele Identifier: CA1310555879

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630213_178630214delinsAT , CM000664.2:g.178630213_178630214delinsAT	GRCh38
NC_000002.11:g.179494940_179494941delinsAT , CM000664.1:g.179494940_179494941delinsAT	GRCh37
NC_000002.10:g.179203185_179203186delinsAT	NCBI36
NG_011618.3:g.205589_205590delinsAT , LRG_391:g.205589_205590delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36577+27_36577+28delinsAT	ENSP00000343764.6:n.36577+27_36577+28deli...
ENST00000342175.11:c.17662+27_17662+28delinsAT	ENSP00000340554.6:n.17662+27_17662+28deli...
ENST00000359218.10:c.17461+27_17461+28delinsAT	ENSP00000352154.5:n.17461+27_17461+28deli...
ENST00000342175.10:c.17662+27_17662+28delinsAT	ENSP00000340554.6:n.17662+27_17662+28deli...
ENST00000342992.10:c.36577+27_36577+28delinsAT	ENSP00000343764.6:n.36577+27_36577+28deli...
ENST00000359218.9:c.17461+27_17461+28delinsAT	ENSP00000352154.5:n.17461+27_17461+28deli...
ENST00000460472.6:c.17086+27_17086+28delinsAT	ENSP00000434586.1:n.17086+27_17086+28deli...
ENST00000589042.5:c.44281+27_44281+28delinsAT MANE Select	ENSP00000467141.1:n.44281+27_44281+28deli...
ENST00000591111.5:c.39358+27_39358+28delinsAT	ENSP00000465570.1:n.39358+27_39358+28deli...
ENST00000615779.4:c.39358+27_39358+28delinsAT	ENSP00000483597.1:n.39358+27_39358+28deli...
NM_001256850.1:c.39358+27_39358+28delinsAT	NP_001243779.1:n.39358+27_39358+28delinsA...
NM_001267550.2:c.44281+27_44281+28delinsAT MANE Select	NP_001254479.2:n.44281+27_44281+28delinsA...
NM_003319.4:c.17086+27_17086+28delinsAT	NP_003310.4:n.17086+27_17086+28delinsAT
NM_133378.4:c.36577+27_36577+28delinsAT	NP_596869.4:n.36577+27_36577+28delinsAT
NM_133432.3:c.17461+27_17461+28delinsAT	NP_597676.3:n.17461+27_17461+28delinsAT
NM_133437.4:c.17662+27_17662+28delinsAT	NP_597681.4:n.17662+27_17662+28delinsAT
XM_011511729.1:c.43378+27_43378+28delinsAT	XP_011510031.1:n.43378+27_43378+28delinsA...
XM_011511730.1:c.17272+27_17272+28delinsAT	XP_011510032.1:n.17272+27_17272+28delinsA...
XM_011511731.1:c.17131+27_17131+28delinsAT	XP_011510033.1:n.17131+27_17131+28delinsA...
XM_017004819.1:c.43174+27_43174+28delinsAT	XP_016860308.1:n.43174+27_43174+28delinsA...
XM_017004820.1:c.38572+27_38572+28delinsAT	XP_016860309.1:n.38572+27_38572+28delinsA...
XM_017004821.1:c.38569+27_38569+28delinsAT	XP_016860310.1:n.38569+27_38569+28delinsA...
XM_017004822.1:c.35611+27_35611+28delinsAT	XP_016860311.1:n.35611+27_35611+28delinsA...
XM_017004823.1:c.17227+27_17227+28delinsAT	XP_016860312.1:n.17227+27_17227+28delinsA...
XM_024453094.1:c.38722+27_38722+28delinsAT	XP_024308862.1:n.38722+27_38722+28delinsA...
XM_024453095.1:c.38719+27_38719+28delinsAT	XP_024308863.1:n.38719+27_38719+28delinsA...
XM_024453096.1:c.38152+27_38152+28delinsAT	XP_024308864.1:n.38152+27_38152+28delinsA...
XM_024453097.1:c.35494+27_35494+28delinsAT	XP_024308865.1:n.35494+27_35494+28delinsA...
XM_024453098.1:c.35413+27_35413+28delinsAT	XP_024308866.1:n.35413+27_35413+28delinsA...
XM_024453099.1:c.17176+27_17176+28delinsAT	XP_024308867.1:n.17176+27_17176+28delinsA...
XM_024453100.1:c.7030+27_7030+28delinsAT	XP_024308868.1:n.7030+27_7030+28delinsAT