Canonical Allele Identifier: CA349450211

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408564A>G (hg19) ; chr2:g.178543837A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543837A>G , CM000664.2:g.178543837A>G	GRCh38
NC_000002.11:g.179408564A>G , CM000664.1:g.179408564A>G	GRCh37
NC_000002.10:g.179116810A>G	NCBI36
NG_011618.3:g.291966T>C , LRG_391:g.291966T>C
NG_051363.1:g.26011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88603T>C (TTN)	ENSP00000343764.6:p.Tyr29535His
ENST00000342175.11:c.69688T>C (TTN)	ENSP00000340554.6:p.Tyr23230His
ENST00000359218.10:c.69487T>C (TTN)	ENSP00000352154.5:p.Tyr23163His
ENST00000342175.10:c.69688T>C (TTN)	ENSP00000340554.6:p.Tyr23230His
ENST00000342992.10:c.88603T>C (TTN)	ENSP00000343764.6:p.Tyr29535His
ENST00000359218.9:c.69487T>C (TTN)	ENSP00000352154.5:p.Tyr23163His
ENST00000460472.6:c.69112T>C (TTN)	ENSP00000434586.1:p.Tyr23038His
ENST00000589042.5:c.96307T>C (TTN) MANE Select	ENSP00000467141.1:p.Tyr32103His
ENST00000591111.5:c.91384T>C (TTN)	ENSP00000465570.1:p.Tyr30462His
ENST00000615779.4:c.91384T>C (TTN)	ENSP00000483597.1:p.Tyr30462His
NM_001256850.1:c.91384T>C (TTN)	NP_001243779.1:p.Tyr30462His
NM_001267550.2:c.96307T>C (TTN) MANE Select	NP_001254479.2:p.Tyr32103His
NM_003319.4:c.69112T>C (TTN)	NP_003310.4:p.Tyr23038His
NM_133378.4:c.88603T>C (TTN)	NP_596869.4:p.Tyr29535His
NM_133432.3:c.69487T>C (TTN)	NP_597676.3:p.Tyr23163His
NM_133437.4:c.69688T>C (TTN)	NP_597681.4:p.Tyr23230His
NR_038271.1:n.446+20201A>G (TTN-AS1)
NR_038272.1:n.2043+1476A>G (TTN-AS1)
XM_011511729.1:c.95404T>C (TTN)	XP_011510031.1:p.Tyr31802His
XM_011511730.1:c.69298T>C (TTN)	XP_011510032.1:p.Tyr23100His
XM_011511731.1:c.69157T>C (TTN)	XP_011510033.1:p.Tyr23053His
XM_017004819.1:c.95200T>C (TTN)	XP_016860308.1:p.Tyr31734His
XM_017004820.1:c.90598T>C (TTN)	XP_016860309.1:p.Tyr30200His
XM_017004821.1:c.90595T>C (TTN)	XP_016860310.1:p.Tyr30199His
XM_017004822.1:c.87637T>C (TTN)	XP_016860311.1:p.Tyr29213His
XM_017004823.1:c.69253T>C (TTN)	XP_016860312.1:p.Tyr23085His
XM_024453094.1:c.90748T>C (TTN)	XP_024308862.1:p.Tyr30250His
XM_024453095.1:c.90745T>C (TTN)	XP_024308863.1:p.Tyr30249His
XM_024453096.1:c.90178T>C (TTN)	XP_024308864.1:p.Tyr30060His
XM_024453097.1:c.87520T>C (TTN)	XP_024308865.1:p.Tyr29174His
XM_024453098.1:c.87439T>C (TTN)	XP_024308866.1:p.Tyr29147His
XM_024453099.1:c.69202T>C (TTN)	XP_024308867.1:p.Tyr23068His
XM_024453100.1:c.59056T>C (TTN)	XP_024308868.1:p.Tyr19686His