Canonical Allele Identifier: CA2503240395

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178624305_178624306insCTCACTGAGTAG , CM000664.2:g.178624305_178624306insCTCACTGAGTAG	GRCh38
NC_000002.11:g.179489032_179489033insCTCACTGAGTAG , CM000664.1:g.179489032_179489033insCTCACTGAGTAG	GRCh37
NC_000002.10:g.179197277_179197278insCTCACTGAGTAG	NCBI36
NG_011618.3:g.211497_211498insCTACTCAGTGAG , LRG_391:g.211497_211498insCTACTCAGTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37111+159_37111+160insCTACTCAGTGAG	ENSP00000343764.6:n.37111+159_37111+160insCTACTCAGTGAG
ENST00000342175.11:c.18196+159_18196+160insCTACTCAGTGAG	ENSP00000340554.6:n.18196+159_18196+160insCTACTCAGTGAG
ENST00000359218.10:c.17995+159_17995+160insCTACTCAGTGAG	ENSP00000352154.5:n.17995+159_17995+160insCTACTCAGTGAG
ENST00000342175.10:c.18196+159_18196+160insCTACTCAGTGAG	ENSP00000340554.6:n.18196+159_18196+160insCTACTCAGTGAG
ENST00000342992.10:c.37111+159_37111+160insCTACTCAGTGAG	ENSP00000343764.6:n.37111+159_37111+160insCTACTCAGTGAG
ENST00000359218.9:c.17995+159_17995+160insCTACTCAGTGAG	ENSP00000352154.5:n.17995+159_17995+160insCTACTCAGTGAG
ENST00000460472.6:c.17620+159_17620+160insCTACTCAGTGAG	ENSP00000434586.1:n.17620+159_17620+160insCTACTCAGTGAG
ENST00000589042.5:c.44815+159_44815+160insCTACTCAGTGAG MANE Select	ENSP00000467141.1:n.44815+159_44815+160insCTACTCAGTGAG
ENST00000591111.5:c.39892+159_39892+160insCTACTCAGTGAG	ENSP00000465570.1:n.39892+159_39892+160insCTACTCAGTGAG
ENST00000615779.4:c.39892+159_39892+160insCTACTCAGTGAG	ENSP00000483597.1:n.39892+159_39892+160insCTACTCAGTGAG
NM_001256850.1:c.39892+159_39892+160insCTACTCAGTGAG	NP_001243779.1:n.39892+159_39892+160insCTACTCAGTGAG
NM_001267550.2:c.44815+159_44815+160insCTACTCAGTGAG MANE Select	NP_001254479.2:n.44815+159_44815+160insCTACTCAGTGAG
NM_003319.4:c.17620+159_17620+160insCTACTCAGTGAG	NP_003310.4:n.17620+159_17620+160insCTACTCAGTGAG
NM_133378.4:c.37111+159_37111+160insCTACTCAGTGAG	NP_596869.4:n.37111+159_37111+160insCTACTCAGTGAG
NM_133432.3:c.17995+159_17995+160insCTACTCAGTGAG	NP_597676.3:n.17995+159_17995+160insCTACTCAGTGAG
NM_133437.4:c.18196+159_18196+160insCTACTCAGTGAG	NP_597681.4:n.18196+159_18196+160insCTACTCAGTGAG
XM_011511729.1:c.43912+159_43912+160insCTACTCAGTGAG	XP_011510031.1:n.43912+159_43912+160insCTACTCAGTGAG
XM_011511730.1:c.17806+159_17806+160insCTACTCAGTGAG	XP_011510032.1:n.17806+159_17806+160insCTACTCAGTGAG
XM_011511731.1:c.17665+159_17665+160insCTACTCAGTGAG	XP_011510033.1:n.17665+159_17665+160insCTACTCAGTGAG
XM_017004819.1:c.43708+159_43708+160insCTACTCAGTGAG	XP_016860308.1:n.43708+159_43708+160insCTACTCAGTGAG
XM_017004820.1:c.39106+159_39106+160insCTACTCAGTGAG	XP_016860309.1:n.39106+159_39106+160insCTACTCAGTGAG
XM_017004821.1:c.39103+159_39103+160insCTACTCAGTGAG	XP_016860310.1:n.39103+159_39103+160insCTACTCAGTGAG
XM_017004822.1:c.36145+159_36145+160insCTACTCAGTGAG	XP_016860311.1:n.36145+159_36145+160insCTACTCAGTGAG
XM_017004823.1:c.17761+159_17761+160insCTACTCAGTGAG	XP_016860312.1:n.17761+159_17761+160insCTACTCAGTGAG
XM_024453094.1:c.39256+159_39256+160insCTACTCAGTGAG	XP_024308862.1:n.39256+159_39256+160insCTACTCAGTGAG
XM_024453095.1:c.39253+159_39253+160insCTACTCAGTGAG	XP_024308863.1:n.39253+159_39253+160insCTACTCAGTGAG
XM_024453096.1:c.38686+159_38686+160insCTACTCAGTGAG	XP_024308864.1:n.38686+159_38686+160insCTACTCAGTGAG
XM_024453097.1:c.36028+159_36028+160insCTACTCAGTGAG	XP_024308865.1:n.36028+159_36028+160insCTACTCAGTGAG
XM_024453098.1:c.35947+159_35947+160insCTACTCAGTGAG	XP_024308866.1:n.35947+159_35947+160insCTACTCAGTGAG
XM_024453099.1:c.17710+159_17710+160insCTACTCAGTGAG	XP_024308867.1:n.17710+159_17710+160insCTACTCAGTGAG
XM_024453100.1:c.7564+159_7564+160insCTACTCAGTGAG	XP_024308868.1:n.7564+159_7564+160insCTACTCAGTGAG