Canonical Allele Identifier: CA1310540509

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591986_178591987delinsTC , CM000664.2:g.178591986_178591987delinsTC	GRCh38
NC_000002.11:g.179456713_179456714delinsTC , CM000664.1:g.179456713_179456714delinsTC	GRCh37
NC_000002.10:g.179164959_179164960delinsTC	NCBI36
NG_011618.3:g.243816_243817delinsGA , LRG_391:g.243816_243817delinsGA
NG_051363.1:g.74160_74161delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52213_52214delinsGA (TTN)	ENSP00000343764.6:p.Asp17405=
ENST00000342175.11:c.33298_33299delinsGA (TTN)	ENSP00000340554.6:p.Asp11100=
ENST00000359218.10:c.33097_33098delinsGA (TTN)	ENSP00000352154.5:p.Asp11033=
ENST00000342175.10:c.33298_33299delinsGA (TTN)	ENSP00000340554.6:p.Asp11100=
ENST00000342992.10:c.52213_52214delinsGA (TTN)	ENSP00000343764.6:p.Asp17405=
ENST00000359218.9:c.33097_33098delinsGA (TTN)	ENSP00000352154.5:p.Asp11033=
ENST00000460472.6:c.32722_32723delinsGA (TTN)	ENSP00000434586.1:p.Asp10908=
ENST00000589042.5:c.59917_59918delinsGA (TTN) MANE Select	ENSP00000467141.1:p.Asp19973=
ENST00000591111.5:c.54994_54995delinsGA (TTN)	ENSP00000465570.1:p.Asp18332=
ENST00000615779.4:c.54994_54995delinsGA (TTN)	ENSP00000483597.1:p.Asp18332=
NM_001256850.1:c.54994_54995delinsGA (TTN)	NP_001243779.1:p.Asp18332=
NM_001267550.2:c.59917_59918delinsGA (TTN) MANE Select	NP_001254479.2:p.Asp19973=
NM_003319.4:c.32722_32723delinsGA (TTN)	NP_003310.4:p.Asp10908=
NM_133378.4:c.52213_52214delinsGA (TTN)	NP_596869.4:p.Asp17405=
NM_133432.3:c.33097_33098delinsGA (TTN)	NP_597676.3:p.Asp11033=
NM_133437.4:c.33298_33299delinsGA (TTN)	NP_597681.4:p.Asp11100=
NR_038271.1:n.597-5610_597-5609delinsTC (TTN-AS1)
NR_038272.1:n.3364+672_3364+673delinsTC (TTN-AS1)
XM_011511729.1:c.59014_59015delinsGA (TTN)	XP_011510031.1:p.Asp19672=
XM_011511730.1:c.32908_32909delinsGA (TTN)	XP_011510032.1:p.Asp10970=
XM_011511731.1:c.32767_32768delinsGA (TTN)	XP_011510033.1:p.Asp10923=
XM_017004819.1:c.58810_58811delinsGA (TTN)	XP_016860308.1:p.Asp19604=
XM_017004820.1:c.54208_54209delinsGA (TTN)	XP_016860309.1:p.Asp18070=
XM_017004821.1:c.54205_54206delinsGA (TTN)	XP_016860310.1:p.Asp18069=
XM_017004822.1:c.51247_51248delinsGA (TTN)	XP_016860311.1:p.Asp17083=
XM_017004823.1:c.32863_32864delinsGA (TTN)	XP_016860312.1:p.Asp10955=
XM_024453094.1:c.54358_54359delinsGA (TTN)	XP_024308862.1:p.Asp18120=
XM_024453095.1:c.54355_54356delinsGA (TTN)	XP_024308863.1:p.Asp18119=
XM_024453096.1:c.53788_53789delinsGA (TTN)	XP_024308864.1:p.Asp17930=
XM_024453097.1:c.51130_51131delinsGA (TTN)	XP_024308865.1:p.Asp17044=
XM_024453098.1:c.51049_51050delinsGA (TTN)	XP_024308866.1:p.Asp17017=
XM_024453099.1:c.32812_32813delinsGA (TTN)	XP_024308867.1:p.Asp10938=
XM_024453100.1:c.22666_22667delinsGA (TTN)	XP_024308868.1:p.Asp7556=