Canonical Allele Identifier: CA2546752935

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530063_178530064insCATAAAAAGCAGTTATT , CM000664.2:g.178530063_178530064insCATAAAAAGCAGTTATT	GRCh38
NC_000002.11:g.179394790_179394791insCATAAAAAGCAGTTATT , CM000664.1:g.179394790_179394791insCATAAAAAGCAGTTATT	GRCh37
NC_000002.10:g.179103036_179103037insCATAAAAAGCAGTTATT	NCBI36
NG_011618.3:g.305739_305740insAATAACTGCTTTTTATG , LRG_391:g.305739_305740insAATAACTGCTTTTTATG
NG_051363.1:g.12237_12238insCATAAAAAGCAGTTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98723_98724insAATAACTGCTTTTTATG (TTN)	ENSP00000343764.6:p.Phe32908LeufsTer8
ENST00000342175.11:c.79808_79809insAATAACTGCTTTTTATG (TTN)	ENSP00000340554.6:p.Phe26603LeufsTer8
ENST00000359218.10:c.79607_79608insAATAACTGCTTTTTATG (TTN)	ENSP00000352154.5:p.Phe26536LeufsTer8
ENST00000342175.10:c.79808_79809insAATAACTGCTTTTTATG (TTN)	ENSP00000340554.6:p.Phe26603LeufsTer8
ENST00000342992.10:c.98723_98724insAATAACTGCTTTTTATG (TTN)	ENSP00000343764.6:p.Phe32908LeufsTer8
ENST00000359218.9:c.79607_79608insAATAACTGCTTTTTATG (TTN)	ENSP00000352154.5:p.Phe26536LeufsTer8
ENST00000460472.6:c.79232_79233insAATAACTGCTTTTTATG (TTN)	ENSP00000434586.1:p.Phe26411LeufsTer8
ENST00000589042.5:c.106427_106428insAATAACTGCTTTTTATG (TTN) MANE Select	ENSP00000467141.1:p.Phe35476LeufsTer8
ENST00000591111.5:c.101504_101505insAATAACTGCTTTTTATG (TTN)	ENSP00000465570.1:p.Phe33835LeufsTer8
ENST00000615779.4:c.101504_101505insAATAACTGCTTTTTATG (TTN)	ENSP00000483597.1:p.Phe33835LeufsTer8
NM_001256850.1:c.101504_101505insAATAACTGCTTTTTATG (TTN)	NP_001243779.1:p.Phe33835LeufsTer8
NM_001267550.2:c.106427_106428insAATAACTGCTTTTTATG (TTN) MANE Select	NP_001254479.2:p.Phe35476LeufsTer8
NM_003319.4:c.79232_79233insAATAACTGCTTTTTATG (TTN)	NP_003310.4:p.Phe26411LeufsTer8
NM_133378.4:c.98723_98724insAATAACTGCTTTTTATG (TTN)	NP_596869.4:p.Phe32908LeufsTer8
NM_133432.3:c.79607_79608insAATAACTGCTTTTTATG (TTN)	NP_597676.3:p.Phe26536LeufsTer8
NM_133437.4:c.79808_79809insAATAACTGCTTTTTATG (TTN)	NP_597681.4:p.Phe26603LeufsTer8
NR_038271.1:n.446+6427_446+6428insCATAAAAAGCAGTTATT (TTN-AS1)
NR_038272.1:n.220-5669_220-5668insCATAAAAAGCAGTTATT (TTN-AS1)
XM_011511729.1:c.105524_105525insAATAACTGCTTTTTATG (TTN)	XP_011510031.1:p.Phe35175LeufsTer8
XM_011511730.1:c.79418_79419insAATAACTGCTTTTTATG (TTN)	XP_011510032.1:p.Phe26473LeufsTer8
XM_011511731.1:c.79277_79278insAATAACTGCTTTTTATG (TTN)	XP_011510033.1:p.Phe26426LeufsTer8
XM_017004819.1:c.105320_105321insAATAACTGCTTTTTATG (TTN)	XP_016860308.1:p.Phe35107LeufsTer8
XM_017004820.1:c.100718_100719insAATAACTGCTTTTTATG (TTN)	XP_016860309.1:p.Phe33573LeufsTer8
XM_017004821.1:c.100715_100716insAATAACTGCTTTTTATG (TTN)	XP_016860310.1:p.Phe33572LeufsTer8
XM_017004822.1:c.97757_97758insAATAACTGCTTTTTATG (TTN)	XP_016860311.1:p.Phe32586LeufsTer8
XM_017004823.1:c.79373_79374insAATAACTGCTTTTTATG (TTN)	XP_016860312.1:p.Phe26458LeufsTer8
XM_024453094.1:c.100868_100869insAATAACTGCTTTTTATG (TTN)	XP_024308862.1:p.Phe33623LeufsTer8
XM_024453095.1:c.100865_100866insAATAACTGCTTTTTATG (TTN)	XP_024308863.1:p.Phe33622LeufsTer8
XM_024453096.1:c.100298_100299insAATAACTGCTTTTTATG (TTN)	XP_024308864.1:p.Phe33433LeufsTer8
XM_024453097.1:c.97640_97641insAATAACTGCTTTTTATG (TTN)	XP_024308865.1:p.Phe32547LeufsTer8
XM_024453098.1:c.97559_97560insAATAACTGCTTTTTATG (TTN)	XP_024308866.1:p.Phe32520LeufsTer8
XM_024453099.1:c.79322_79323insAATAACTGCTTTTTATG (TTN)	XP_024308867.1:p.Phe26441LeufsTer8
XM_024453100.1:c.69176_69177insAATAACTGCTTTTTATG (TTN)	XP_024308868.1:p.Phe23059LeufsTer8