Canonical Allele Identifier: CA1310518106

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532160_178532163delinsATTC , CM000664.2:g.178532160_178532163delinsATTC	GRCh38
NC_000002.11:g.179396887_179396890delinsATTC , CM000664.1:g.179396887_179396890delinsATTC	GRCh37
NC_000002.10:g.179105133_179105136delinsATTC	NCBI36
NG_011618.3:g.303640_303643delinsGAAT , LRG_391:g.303640_303643delinsGAAT
NG_051363.1:g.14334_14337delinsATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96748_96751delinsGAAT (TTN)	ENSP00000343764.6:p.Glu32250=
ENST00000342175.11:c.77833_77836delinsGAAT (TTN)	ENSP00000340554.6:p.Glu25945=
ENST00000359218.10:c.77632_77635delinsGAAT (TTN)	ENSP00000352154.5:p.Glu25878=
ENST00000342175.10:c.77833_77836delinsGAAT (TTN)	ENSP00000340554.6:p.Glu25945=
ENST00000342992.10:c.96748_96751delinsGAAT (TTN)	ENSP00000343764.6:p.Glu32250=
ENST00000359218.9:c.77632_77635delinsGAAT (TTN)	ENSP00000352154.5:p.Glu25878=
ENST00000460472.6:c.77257_77260delinsGAAT (TTN)	ENSP00000434586.1:p.Glu25753=
ENST00000589042.5:c.104452_104455delinsGAAT (TTN) MANE Select	ENSP00000467141.1:p.Glu34818=
ENST00000591111.5:c.99529_99532delinsGAAT (TTN)	ENSP00000465570.1:p.Glu33177=
ENST00000615779.4:c.99529_99532delinsGAAT (TTN)	ENSP00000483597.1:p.Glu33177=
NM_001256850.1:c.99529_99532delinsGAAT (TTN)	NP_001243779.1:p.Glu33177=
NM_001267550.2:c.104452_104455delinsGAAT (TTN) MANE Select	NP_001254479.2:p.Glu34818=
NM_003319.4:c.77257_77260delinsGAAT (TTN)	NP_003310.4:p.Glu25753=
NM_133378.4:c.96748_96751delinsGAAT (TTN)	NP_596869.4:p.Glu32250=
NM_133432.3:c.77632_77635delinsGAAT (TTN)	NP_597676.3:p.Glu25878=
NM_133437.4:c.77833_77836delinsGAAT (TTN)	NP_597681.4:p.Glu25945=
NR_038271.1:n.446+8524_446+8527delinsATTC (TTN-AS1)
NR_038272.1:n.220-3572_220-3569delinsATTC (TTN-AS1)
XM_011511729.1:c.103549_103552delinsGAAT (TTN)	XP_011510031.1:p.Glu34517=
XM_011511730.1:c.77443_77446delinsGAAT (TTN)	XP_011510032.1:p.Glu25815=
XM_011511731.1:c.77302_77305delinsGAAT (TTN)	XP_011510033.1:p.Glu25768=
XM_017004819.1:c.103345_103348delinsGAAT (TTN)	XP_016860308.1:p.Glu34449=
XM_017004820.1:c.98743_98746delinsGAAT (TTN)	XP_016860309.1:p.Glu32915=
XM_017004821.1:c.98740_98743delinsGAAT (TTN)	XP_016860310.1:p.Glu32914=
XM_017004822.1:c.95782_95785delinsGAAT (TTN)	XP_016860311.1:p.Glu31928=
XM_017004823.1:c.77398_77401delinsGAAT (TTN)	XP_016860312.1:p.Glu25800=
XM_024453094.1:c.98893_98896delinsGAAT (TTN)	XP_024308862.1:p.Glu32965=
XM_024453095.1:c.98890_98893delinsGAAT (TTN)	XP_024308863.1:p.Glu32964=
XM_024453096.1:c.98323_98326delinsGAAT (TTN)	XP_024308864.1:p.Glu32775=
XM_024453097.1:c.95665_95668delinsGAAT (TTN)	XP_024308865.1:p.Glu31889=
XM_024453098.1:c.95584_95587delinsGAAT (TTN)	XP_024308866.1:p.Glu31862=
XM_024453099.1:c.77347_77350delinsGAAT (TTN)	XP_024308867.1:p.Glu25783=
XM_024453100.1:c.67201_67204delinsGAAT (TTN)	XP_024308868.1:p.Glu22401=