Canonical Allele Identifier: CA349407166

Gene: TTN TTN-AS1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98335A>G (TTN)	ENSP00000343764.6:p.Asn32779Asp
ENST00000342175.11:c.79420A>G (TTN)	ENSP00000340554.6:p.Asn26474Asp
ENST00000359218.10:c.79219A>G (TTN)	ENSP00000352154.5:p.Asn26407Asp
ENST00000342175.10:c.79420A>G (TTN)	ENSP00000340554.6:p.Asn26474Asp
ENST00000342992.10:c.98335A>G (TTN)	ENSP00000343764.6:p.Asn32779Asp
ENST00000359218.9:c.79219A>G (TTN)	ENSP00000352154.5:p.Asn26407Asp
ENST00000460472.6:c.78844A>G (TTN)	ENSP00000434586.1:p.Asn26282Asp
ENST00000589042.5:c.106039A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn35347Asp
ENST00000591111.5:c.101116A>G (TTN)	ENSP00000465570.1:p.Asn33706Asp
ENST00000615779.4:c.101116A>G (TTN)	ENSP00000483597.1:p.Asn33706Asp
NM_001256850.1:c.101116A>G (TTN)	NP_001243779.1:p.Asn33706Asp
NM_001267550.2:c.106039A>G (TTN) MANE Select	NP_001254479.2:p.Asn35347Asp
NM_003319.4:c.78844A>G (TTN)	NP_003310.4:p.Asn26282Asp
NM_133378.4:c.98335A>G (TTN)	NP_596869.4:p.Asn32779Asp
NM_133432.3:c.79219A>G (TTN)	NP_597676.3:p.Asn26407Asp
NM_133437.4:c.79420A>G (TTN)	NP_597681.4:p.Asn26474Asp
NR_038271.1:n.446+6940T>C (TTN-AS1)
NR_038272.1:n.220-5156T>C (TTN-AS1)
XM_011511729.1:c.105136A>G (TTN)	XP_011510031.1:p.Asn35046Asp
XM_011511730.1:c.79030A>G (TTN)	XP_011510032.1:p.Asn26344Asp
XM_011511731.1:c.78889A>G (TTN)	XP_011510033.1:p.Asn26297Asp
XM_017004819.1:c.104932A>G (TTN)	XP_016860308.1:p.Asn34978Asp
XM_017004820.1:c.100330A>G (TTN)	XP_016860309.1:p.Asn33444Asp
XM_017004821.1:c.100327A>G (TTN)	XP_016860310.1:p.Asn33443Asp
XM_017004822.1:c.97369A>G (TTN)	XP_016860311.1:p.Asn32457Asp
XM_017004823.1:c.78985A>G (TTN)	XP_016860312.1:p.Asn26329Asp
XM_024453094.1:c.100480A>G (TTN)	XP_024308862.1:p.Asn33494Asp
XM_024453095.1:c.100477A>G (TTN)	XP_024308863.1:p.Asn33493Asp
XM_024453096.1:c.99910A>G (TTN)	XP_024308864.1:p.Asn33304Asp
XM_024453097.1:c.97252A>G (TTN)	XP_024308865.1:p.Asn32418Asp
XM_024453098.1:c.97171A>G (TTN)	XP_024308866.1:p.Asn32391Asp
XM_024453099.1:c.78934A>G (TTN)	XP_024308867.1:p.Asn26312Asp
XM_024453100.1:c.68788A>G (TTN)	XP_024308868.1:p.Asn22930Asp