Canonical Allele Identifier: CA2017999286

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530563del , CM000664.2:g.178530563del	GRCh38
NC_000002.11:g.179395290del , CM000664.1:g.179395290del	GRCh37
NC_000002.10:g.179103536del	NCBI36
NG_011618.3:g.305241del , LRG_391:g.305241del
NG_051363.1:g.12737del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98349del (TTN)	ENSP00000343764.6:p.Glu32783AspfsTer?
ENST00000342175.11:c.79434del (TTN)	ENSP00000340554.6:p.Glu26478AspfsTer?
ENST00000359218.10:c.79233del (TTN)	ENSP00000352154.5:p.Glu26411AspfsTer?
ENST00000342175.10:c.79434del (TTN)	ENSP00000340554.6:p.Glu26478AspfsTer?
ENST00000342992.10:c.98349del (TTN)	ENSP00000343764.6:p.Glu32783AspfsTer?
ENST00000359218.9:c.79233del (TTN)	ENSP00000352154.5:p.Glu26411AspfsTer?
ENST00000460472.6:c.78858del (TTN)	ENSP00000434586.1:p.Glu26286AspfsTer?
ENST00000589042.5:c.106053del (TTN) MANE Select	ENSP00000467141.1:p.Glu35351AspfsTer?
ENST00000591111.5:c.101130del (TTN)	ENSP00000465570.1:p.Glu33710AspfsTer?
ENST00000615779.4:c.101130del (TTN)	ENSP00000483597.1:p.Glu33710AspfsTer?
NM_001256850.1:c.101130del (TTN)	NP_001243779.1:p.Glu33710AspfsTer?
NM_001267550.2:c.106053del (TTN) MANE Select	NP_001254479.2:p.Glu35351AspfsTer?
NM_003319.4:c.78858del (TTN)	NP_003310.4:p.Glu26286AspfsTer?
NM_133378.4:c.98349del (TTN)	NP_596869.4:p.Glu32783AspfsTer?
NM_133432.3:c.79233del (TTN)	NP_597676.3:p.Glu26411AspfsTer?
NM_133437.4:c.79434del (TTN)	NP_597681.4:p.Glu26478AspfsTer?
NR_038271.1:n.446+6927del (TTN-AS1)
NR_038272.1:n.220-5169del (TTN-AS1)
XM_011511729.1:c.105150del (TTN)	XP_011510031.1:p.Glu35050AspfsTer?
XM_011511730.1:c.79044del (TTN)	XP_011510032.1:p.Glu26348AspfsTer?
XM_011511731.1:c.78903del (TTN)	XP_011510033.1:p.Glu26301AspfsTer?
XM_017004819.1:c.104946del (TTN)	XP_016860308.1:p.Glu34982AspfsTer?
XM_017004820.1:c.100344del (TTN)	XP_016860309.1:p.Glu33448AspfsTer?
XM_017004821.1:c.100341del (TTN)	XP_016860310.1:p.Glu33447AspfsTer?
XM_017004822.1:c.97383del (TTN)	XP_016860311.1:p.Glu32461AspfsTer?
XM_017004823.1:c.78999del (TTN)	XP_016860312.1:p.Glu26333AspfsTer?
XM_024453094.1:c.100494del (TTN)	XP_024308862.1:p.Glu33498AspfsTer?
XM_024453095.1:c.100491del (TTN)	XP_024308863.1:p.Glu33497AspfsTer?
XM_024453096.1:c.99924del (TTN)	XP_024308864.1:p.Glu33308AspfsTer?
XM_024453097.1:c.97266del (TTN)	XP_024308865.1:p.Glu32422AspfsTer?
XM_024453098.1:c.97185del (TTN)	XP_024308866.1:p.Glu32395AspfsTer?
XM_024453099.1:c.78948del (TTN)	XP_024308867.1:p.Glu26316AspfsTer?
XM_024453100.1:c.68802del (TTN)	XP_024308868.1:p.Glu22934AspfsTer?