Canonical Allele Identifier: CA1310555839

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630133_178630134delinsGT , CM000664.2:g.178630133_178630134delinsGT	GRCh38
NC_000002.11:g.179494860_179494861delinsGT , CM000664.1:g.179494860_179494861delinsGT	GRCh37
NC_000002.10:g.179203105_179203106delinsGT	NCBI36
NG_011618.3:g.205669_205670delinsAC , LRG_391:g.205669_205670delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36577+107_36577+108delinsAC	ENSP00000343764.6:n.36577+107_36577+108delinsAC
ENST00000342175.11:c.17662+107_17662+108delinsAC	ENSP00000340554.6:n.17662+107_17662+108delinsAC
ENST00000359218.10:c.17461+107_17461+108delinsAC	ENSP00000352154.5:n.17461+107_17461+108delinsAC
ENST00000342175.10:c.17662+107_17662+108delinsAC	ENSP00000340554.6:n.17662+107_17662+108delinsAC
ENST00000342992.10:c.36577+107_36577+108delinsAC	ENSP00000343764.6:n.36577+107_36577+108delinsAC
ENST00000359218.9:c.17461+107_17461+108delinsAC	ENSP00000352154.5:n.17461+107_17461+108delinsAC
ENST00000460472.6:c.17086+107_17086+108delinsAC	ENSP00000434586.1:n.17086+107_17086+108delinsAC
ENST00000589042.5:c.44281+107_44281+108delinsAC MANE Select	ENSP00000467141.1:n.44281+107_44281+108delinsAC
ENST00000591111.5:c.39358+107_39358+108delinsAC	ENSP00000465570.1:n.39358+107_39358+108delinsAC
ENST00000615779.4:c.39358+107_39358+108delinsAC	ENSP00000483597.1:n.39358+107_39358+108delinsAC
NM_001256850.1:c.39358+107_39358+108delinsAC	NP_001243779.1:n.39358+107_39358+108delinsAC
NM_001267550.2:c.44281+107_44281+108delinsAC MANE Select	NP_001254479.2:n.44281+107_44281+108delinsAC
NM_003319.4:c.17086+107_17086+108delinsAC	NP_003310.4:n.17086+107_17086+108delinsAC
NM_133378.4:c.36577+107_36577+108delinsAC	NP_596869.4:n.36577+107_36577+108delinsAC
NM_133432.3:c.17461+107_17461+108delinsAC	NP_597676.3:n.17461+107_17461+108delinsAC
NM_133437.4:c.17662+107_17662+108delinsAC	NP_597681.4:n.17662+107_17662+108delinsAC
XM_011511729.1:c.43378+107_43378+108delinsAC	XP_011510031.1:n.43378+107_43378+108delinsAC
XM_011511730.1:c.17272+107_17272+108delinsAC	XP_011510032.1:n.17272+107_17272+108delinsAC
XM_011511731.1:c.17131+107_17131+108delinsAC	XP_011510033.1:n.17131+107_17131+108delinsAC
XM_017004819.1:c.43174+107_43174+108delinsAC	XP_016860308.1:n.43174+107_43174+108delinsAC
XM_017004820.1:c.38572+107_38572+108delinsAC	XP_016860309.1:n.38572+107_38572+108delinsAC
XM_017004821.1:c.38569+107_38569+108delinsAC	XP_016860310.1:n.38569+107_38569+108delinsAC
XM_017004822.1:c.35611+107_35611+108delinsAC	XP_016860311.1:n.35611+107_35611+108delinsAC
XM_017004823.1:c.17227+107_17227+108delinsAC	XP_016860312.1:n.17227+107_17227+108delinsAC
XM_024453094.1:c.38722+107_38722+108delinsAC	XP_024308862.1:n.38722+107_38722+108delinsAC
XM_024453095.1:c.38719+107_38719+108delinsAC	XP_024308863.1:n.38719+107_38719+108delinsAC
XM_024453096.1:c.38152+107_38152+108delinsAC	XP_024308864.1:n.38152+107_38152+108delinsAC
XM_024453097.1:c.35494+107_35494+108delinsAC	XP_024308865.1:n.35494+107_35494+108delinsAC
XM_024453098.1:c.35413+107_35413+108delinsAC	XP_024308866.1:n.35413+107_35413+108delinsAC
XM_024453099.1:c.17176+107_17176+108delinsAC	XP_024308867.1:n.17176+107_17176+108delinsAC
XM_024453100.1:c.7030+107_7030+108delinsAC	XP_024308868.1:n.7030+107_7030+108delinsAC