Canonical Allele Identifier: CA2586965336

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178573869del , CM000664.2:g.178573869del	GRCh38
NC_000002.11:g.179438596del , CM000664.1:g.179438596del	GRCh37
NC_000002.10:g.179146842del	NCBI36
NG_011618.3:g.261934del , LRG_391:g.261934del
NG_051363.1:g.56043del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.64559del (TTN)	ENSP00000343764.6:p.Val21520GlufsTer?
ENST00000342175.11:c.45644del (TTN)	ENSP00000340554.6:p.Val15215GlufsTer?
ENST00000359218.10:c.45443del (TTN)	ENSP00000352154.5:p.Val15148GlufsTer?
ENST00000342175.10:c.45644del (TTN)	ENSP00000340554.6:p.Val15215GlufsTer?
ENST00000342992.10:c.64559del (TTN)	ENSP00000343764.6:p.Val21520GlufsTer?
ENST00000359218.9:c.45443del (TTN)	ENSP00000352154.5:p.Val15148GlufsTer?
ENST00000460472.6:c.45068del (TTN)	ENSP00000434586.1:p.Val15023GlufsTer?
ENST00000589042.5:c.72263del (TTN) MANE Select	ENSP00000467141.1:p.Val24088GlufsTer?
ENST00000591111.5:c.67340del (TTN)	ENSP00000465570.1:p.Val22447GlufsTer?
ENST00000615779.4:c.67340del (TTN)	ENSP00000483597.1:p.Val22447GlufsTer?
NM_001256850.1:c.67340del (TTN)	NP_001243779.1:p.Val22447GlufsTer?
NM_001267550.2:c.72263del (TTN) MANE Select	NP_001254479.2:p.Val24088GlufsTer?
NM_003319.4:c.45068del (TTN)	NP_003310.4:p.Val15023GlufsTer?
NM_133378.4:c.64559del (TTN)	NP_596869.4:p.Val21520GlufsTer?
NM_133432.3:c.45443del (TTN)	NP_597676.3:p.Val15148GlufsTer?
NM_133437.4:c.45644del (TTN)	NP_597681.4:p.Val15215GlufsTer?
NR_038271.1:n.596+2420del (TTN-AS1)
NR_038272.1:n.2044-8703del (TTN-AS1)
XM_011511729.1:c.71360del (TTN)	XP_011510031.1:p.Val23787GlufsTer?
XM_011511730.1:c.45254del (TTN)	XP_011510032.1:p.Val15085GlufsTer?
XM_011511731.1:c.45113del (TTN)	XP_011510033.1:p.Val15038GlufsTer?
XM_017004819.1:c.71156del (TTN)	XP_016860308.1:p.Val23719GlufsTer?
XM_017004820.1:c.66554del (TTN)	XP_016860309.1:p.Val22185GlufsTer?
XM_017004821.1:c.66551del (TTN)	XP_016860310.1:p.Val22184GlufsTer?
XM_017004822.1:c.63593del (TTN)	XP_016860311.1:p.Val21198GlufsTer?
XM_017004823.1:c.45209del (TTN)	XP_016860312.1:p.Val15070GlufsTer?
XM_024453094.1:c.66704del (TTN)	XP_024308862.1:p.Val22235GlufsTer?
XM_024453095.1:c.66701del (TTN)	XP_024308863.1:p.Val22234GlufsTer?
XM_024453096.1:c.66134del (TTN)	XP_024308864.1:p.Val22045GlufsTer?
XM_024453097.1:c.63476del (TTN)	XP_024308865.1:p.Val21159GlufsTer?
XM_024453098.1:c.63395del (TTN)	XP_024308866.1:p.Val21132GlufsTer?
XM_024453099.1:c.45158del (TTN)	XP_024308867.1:p.Val15053GlufsTer?
XM_024453100.1:c.35012del (TTN)	XP_024308868.1:p.Val11671GlufsTer?