Canonical Allele Identifier: CA349407165

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395303T>A (hg19) ; chr2:g.178530576T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530576T>A , CM000664.2:g.178530576T>A	GRCh38
NC_000002.11:g.179395303T>A , CM000664.1:g.179395303T>A	GRCh37
NC_000002.10:g.179103549T>A	NCBI36
NG_011618.3:g.305227A>T , LRG_391:g.305227A>T
NG_051363.1:g.12750T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98335A>T (TTN)	ENSP00000343764.6:p.Asn32779Tyr
ENST00000342175.11:c.79420A>T (TTN)	ENSP00000340554.6:p.Asn26474Tyr
ENST00000359218.10:c.79219A>T (TTN)	ENSP00000352154.5:p.Asn26407Tyr
ENST00000342175.10:c.79420A>T (TTN)	ENSP00000340554.6:p.Asn26474Tyr
ENST00000342992.10:c.98335A>T (TTN)	ENSP00000343764.6:p.Asn32779Tyr
ENST00000359218.9:c.79219A>T (TTN)	ENSP00000352154.5:p.Asn26407Tyr
ENST00000460472.6:c.78844A>T (TTN)	ENSP00000434586.1:p.Asn26282Tyr
ENST00000589042.5:c.106039A>T (TTN) MANE Select	ENSP00000467141.1:p.Asn35347Tyr
ENST00000591111.5:c.101116A>T (TTN)	ENSP00000465570.1:p.Asn33706Tyr
ENST00000615779.4:c.101116A>T (TTN)	ENSP00000483597.1:p.Asn33706Tyr
NM_001256850.1:c.101116A>T (TTN)	NP_001243779.1:p.Asn33706Tyr
NM_001267550.2:c.106039A>T (TTN) MANE Select	NP_001254479.2:p.Asn35347Tyr
NM_003319.4:c.78844A>T (TTN)	NP_003310.4:p.Asn26282Tyr
NM_133378.4:c.98335A>T (TTN)	NP_596869.4:p.Asn32779Tyr
NM_133432.3:c.79219A>T (TTN)	NP_597676.3:p.Asn26407Tyr
NM_133437.4:c.79420A>T (TTN)	NP_597681.4:p.Asn26474Tyr
NR_038271.1:n.446+6940T>A (TTN-AS1)
NR_038272.1:n.220-5156T>A (TTN-AS1)
XM_011511729.1:c.105136A>T (TTN)	XP_011510031.1:p.Asn35046Tyr
XM_011511730.1:c.79030A>T (TTN)	XP_011510032.1:p.Asn26344Tyr
XM_011511731.1:c.78889A>T (TTN)	XP_011510033.1:p.Asn26297Tyr
XM_017004819.1:c.104932A>T (TTN)	XP_016860308.1:p.Asn34978Tyr
XM_017004820.1:c.100330A>T (TTN)	XP_016860309.1:p.Asn33444Tyr
XM_017004821.1:c.100327A>T (TTN)	XP_016860310.1:p.Asn33443Tyr
XM_017004822.1:c.97369A>T (TTN)	XP_016860311.1:p.Asn32457Tyr
XM_017004823.1:c.78985A>T (TTN)	XP_016860312.1:p.Asn26329Tyr
XM_024453094.1:c.100480A>T (TTN)	XP_024308862.1:p.Asn33494Tyr
XM_024453095.1:c.100477A>T (TTN)	XP_024308863.1:p.Asn33493Tyr
XM_024453096.1:c.99910A>T (TTN)	XP_024308864.1:p.Asn33304Tyr
XM_024453097.1:c.97252A>T (TTN)	XP_024308865.1:p.Asn32418Tyr
XM_024453098.1:c.97171A>T (TTN)	XP_024308866.1:p.Asn32391Tyr
XM_024453099.1:c.78934A>T (TTN)	XP_024308867.1:p.Asn26312Tyr
XM_024453100.1:c.68788A>T (TTN)	XP_024308868.1:p.Asn22930Tyr