Canonical Allele Identifier: CA1310555851

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630153_178630157delinsCTAAT , CM000664.2:g.178630153_178630157delinsCTAAT	GRCh38
NC_000002.11:g.179494880_179494884delinsCTAAT , CM000664.1:g.179494880_179494884delinsCTAAT	GRCh37
NC_000002.10:g.179203125_179203129delinsCTAAT	NCBI36
NG_011618.3:g.205646_205650delinsATTAG , LRG_391:g.205646_205650delinsATTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.36577+84_36577+88delinsATTAG	ENSP00000343764.6:n.36577+84_36577+88delinsATTAG
ENST00000342175.11:c.17662+84_17662+88delinsATTAG	ENSP00000340554.6:n.17662+84_17662+88delinsATTAG
ENST00000359218.10:c.17461+84_17461+88delinsATTAG	ENSP00000352154.5:n.17461+84_17461+88delinsATTAG
ENST00000342175.10:c.17662+84_17662+88delinsATTAG	ENSP00000340554.6:n.17662+84_17662+88delinsATTAG
ENST00000342992.10:c.36577+84_36577+88delinsATTAG	ENSP00000343764.6:n.36577+84_36577+88delinsATTAG
ENST00000359218.9:c.17461+84_17461+88delinsATTAG	ENSP00000352154.5:n.17461+84_17461+88delinsATTAG
ENST00000460472.6:c.17086+84_17086+88delinsATTAG	ENSP00000434586.1:n.17086+84_17086+88delinsATTAG
ENST00000589042.5:c.44281+84_44281+88delinsATTAG MANE Select	ENSP00000467141.1:n.44281+84_44281+88delinsATTAG
ENST00000591111.5:c.39358+84_39358+88delinsATTAG	ENSP00000465570.1:n.39358+84_39358+88delinsATTAG
ENST00000615779.4:c.39358+84_39358+88delinsATTAG	ENSP00000483597.1:n.39358+84_39358+88delinsATTAG
NM_001256850.1:c.39358+84_39358+88delinsATTAG	NP_001243779.1:n.39358+84_39358+88delinsATTAG
NM_001267550.2:c.44281+84_44281+88delinsATTAG MANE Select	NP_001254479.2:n.44281+84_44281+88delinsATTAG
NM_003319.4:c.17086+84_17086+88delinsATTAG	NP_003310.4:n.17086+84_17086+88delinsATTAG
NM_133378.4:c.36577+84_36577+88delinsATTAG	NP_596869.4:n.36577+84_36577+88delinsATTAG
NM_133432.3:c.17461+84_17461+88delinsATTAG	NP_597676.3:n.17461+84_17461+88delinsATTAG
NM_133437.4:c.17662+84_17662+88delinsATTAG	NP_597681.4:n.17662+84_17662+88delinsATTAG
XM_011511729.1:c.43378+84_43378+88delinsATTAG	XP_011510031.1:n.43378+84_43378+88delinsATTAG
XM_011511730.1:c.17272+84_17272+88delinsATTAG	XP_011510032.1:n.17272+84_17272+88delinsATTAG
XM_011511731.1:c.17131+84_17131+88delinsATTAG	XP_011510033.1:n.17131+84_17131+88delinsATTAG
XM_017004819.1:c.43174+84_43174+88delinsATTAG	XP_016860308.1:n.43174+84_43174+88delinsATTAG
XM_017004820.1:c.38572+84_38572+88delinsATTAG	XP_016860309.1:n.38572+84_38572+88delinsATTAG
XM_017004821.1:c.38569+84_38569+88delinsATTAG	XP_016860310.1:n.38569+84_38569+88delinsATTAG
XM_017004822.1:c.35611+84_35611+88delinsATTAG	XP_016860311.1:n.35611+84_35611+88delinsATTAG
XM_017004823.1:c.17227+84_17227+88delinsATTAG	XP_016860312.1:n.17227+84_17227+88delinsATTAG
XM_024453094.1:c.38722+84_38722+88delinsATTAG	XP_024308862.1:n.38722+84_38722+88delinsATTAG
XM_024453095.1:c.38719+84_38719+88delinsATTAG	XP_024308863.1:n.38719+84_38719+88delinsATTAG
XM_024453096.1:c.38152+84_38152+88delinsATTAG	XP_024308864.1:n.38152+84_38152+88delinsATTAG
XM_024453097.1:c.35494+84_35494+88delinsATTAG	XP_024308865.1:n.35494+84_35494+88delinsATTAG
XM_024453098.1:c.35413+84_35413+88delinsATTAG	XP_024308866.1:n.35413+84_35413+88delinsATTAG
XM_024453099.1:c.17176+84_17176+88delinsATTAG	XP_024308867.1:n.17176+84_17176+88delinsATTAG
XM_024453100.1:c.7030+84_7030+88delinsATTAG	XP_024308868.1:n.7030+84_7030+88delinsATTAG