Canonical Allele Identifier: CA1310514804

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530599_178530600delinsTC , CM000664.2:g.178530599_178530600delinsTC	GRCh38
NC_000002.11:g.179395326_179395327delinsTC , CM000664.1:g.179395326_179395327delinsTC	GRCh37
NC_000002.10:g.179103572_179103573delinsTC	NCBI36
NG_011618.3:g.305203_305204delinsGA , LRG_391:g.305203_305204delinsGA
NG_051363.1:g.12773_12774delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98311_98312delinsGA (TTN)	ENSP00000343764.6:p.Asp32771=
ENST00000342175.11:c.79396_79397delinsGA (TTN)	ENSP00000340554.6:p.Asp26466=
ENST00000359218.10:c.79195_79196delinsGA (TTN)	ENSP00000352154.5:p.Asp26399=
ENST00000342175.10:c.79396_79397delinsGA (TTN)	ENSP00000340554.6:p.Asp26466=
ENST00000342992.10:c.98311_98312delinsGA (TTN)	ENSP00000343764.6:p.Asp32771=
ENST00000359218.9:c.79195_79196delinsGA (TTN)	ENSP00000352154.5:p.Asp26399=
ENST00000460472.6:c.78820_78821delinsGA (TTN)	ENSP00000434586.1:p.Asp26274=
ENST00000589042.5:c.106015_106016delinsGA (TTN) MANE Select	ENSP00000467141.1:p.Asp35339=
ENST00000591111.5:c.101092_101093delinsGA (TTN)	ENSP00000465570.1:p.Asp33698=
ENST00000615779.4:c.101092_101093delinsGA (TTN)	ENSP00000483597.1:p.Asp33698=
NM_001256850.1:c.101092_101093delinsGA (TTN)	NP_001243779.1:p.Asp33698=
NM_001267550.2:c.106015_106016delinsGA (TTN) MANE Select	NP_001254479.2:p.Asp35339=
NM_003319.4:c.78820_78821delinsGA (TTN)	NP_003310.4:p.Asp26274=
NM_133378.4:c.98311_98312delinsGA (TTN)	NP_596869.4:p.Asp32771=
NM_133432.3:c.79195_79196delinsGA (TTN)	NP_597676.3:p.Asp26399=
NM_133437.4:c.79396_79397delinsGA (TTN)	NP_597681.4:p.Asp26466=
NR_038271.1:n.446+6963_446+6964delinsTC (TTN-AS1)
NR_038272.1:n.220-5133_220-5132delinsTC (TTN-AS1)
XM_011511729.1:c.105112_105113delinsGA (TTN)	XP_011510031.1:p.Asp35038=
XM_011511730.1:c.79006_79007delinsGA (TTN)	XP_011510032.1:p.Asp26336=
XM_011511731.1:c.78865_78866delinsGA (TTN)	XP_011510033.1:p.Asp26289=
XM_017004819.1:c.104908_104909delinsGA (TTN)	XP_016860308.1:p.Asp34970=
XM_017004820.1:c.100306_100307delinsGA (TTN)	XP_016860309.1:p.Asp33436=
XM_017004821.1:c.100303_100304delinsGA (TTN)	XP_016860310.1:p.Asp33435=
XM_017004822.1:c.97345_97346delinsGA (TTN)	XP_016860311.1:p.Asp32449=
XM_017004823.1:c.78961_78962delinsGA (TTN)	XP_016860312.1:p.Asp26321=
XM_024453094.1:c.100456_100457delinsGA (TTN)	XP_024308862.1:p.Asp33486=
XM_024453095.1:c.100453_100454delinsGA (TTN)	XP_024308863.1:p.Asp33485=
XM_024453096.1:c.99886_99887delinsGA (TTN)	XP_024308864.1:p.Asp33296=
XM_024453097.1:c.97228_97229delinsGA (TTN)	XP_024308865.1:p.Asp32410=
XM_024453098.1:c.97147_97148delinsGA (TTN)	XP_024308866.1:p.Asp32383=
XM_024453099.1:c.78910_78911delinsGA (TTN)	XP_024308867.1:p.Asp26304=
XM_024453100.1:c.68764_68765delinsGA (TTN)	XP_024308868.1:p.Asp22922=