Canonical Allele Identifier: CA349456708

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409095T>A (hg19) ; chr2:g.178544368T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544368T>A , CM000664.2:g.178544368T>A	GRCh38
NC_000002.11:g.179409095T>A , CM000664.1:g.179409095T>A	GRCh37
NC_000002.10:g.179117341T>A	NCBI36
NG_011618.3:g.291435A>T , LRG_391:g.291435A>T
NG_051363.1:g.26542T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88157A>T (TTN)	ENSP00000343764.6:p.Asp29386Val
ENST00000342175.11:c.69242A>T (TTN)	ENSP00000340554.6:p.Asp23081Val
ENST00000359218.10:c.69041A>T (TTN)	ENSP00000352154.5:p.Asp23014Val
ENST00000342175.10:c.69242A>T (TTN)	ENSP00000340554.6:p.Asp23081Val
ENST00000342992.10:c.88157A>T (TTN)	ENSP00000343764.6:p.Asp29386Val
ENST00000359218.9:c.69041A>T (TTN)	ENSP00000352154.5:p.Asp23014Val
ENST00000460472.6:c.68666A>T (TTN)	ENSP00000434586.1:p.Asp22889Val
ENST00000589042.5:c.95861A>T (TTN) MANE Select	ENSP00000467141.1:p.Asp31954Val
ENST00000591111.5:c.90938A>T (TTN)	ENSP00000465570.1:p.Asp30313Val
ENST00000615779.4:c.90938A>T (TTN)	ENSP00000483597.1:p.Asp30313Val
NM_001256850.1:c.90938A>T (TTN)	NP_001243779.1:p.Asp30313Val
NM_001267550.2:c.95861A>T (TTN) MANE Select	NP_001254479.2:p.Asp31954Val
NM_003319.4:c.68666A>T (TTN)	NP_003310.4:p.Asp22889Val
NM_133378.4:c.88157A>T (TTN)	NP_596869.4:p.Asp29386Val
NM_133432.3:c.69041A>T (TTN)	NP_597676.3:p.Asp23014Val
NM_133437.4:c.69242A>T (TTN)	NP_597681.4:p.Asp23081Val
NR_038271.1:n.446+20732T>A (TTN-AS1)
NR_038272.1:n.2043+2007T>A (TTN-AS1)
XM_011511729.1:c.94958A>T (TTN)	XP_011510031.1:p.Asp31653Val
XM_011511730.1:c.68852A>T (TTN)	XP_011510032.1:p.Asp22951Val
XM_011511731.1:c.68711A>T (TTN)	XP_011510033.1:p.Asp22904Val
XM_017004819.1:c.94754A>T (TTN)	XP_016860308.1:p.Asp31585Val
XM_017004820.1:c.90152A>T (TTN)	XP_016860309.1:p.Asp30051Val
XM_017004821.1:c.90149A>T (TTN)	XP_016860310.1:p.Asp30050Val
XM_017004822.1:c.87191A>T (TTN)	XP_016860311.1:p.Asp29064Val
XM_017004823.1:c.68807A>T (TTN)	XP_016860312.1:p.Asp22936Val
XM_024453094.1:c.90302A>T (TTN)	XP_024308862.1:p.Asp30101Val
XM_024453095.1:c.90299A>T (TTN)	XP_024308863.1:p.Asp30100Val
XM_024453096.1:c.89732A>T (TTN)	XP_024308864.1:p.Asp29911Val
XM_024453097.1:c.87074A>T (TTN)	XP_024308865.1:p.Asp29025Val
XM_024453098.1:c.86993A>T (TTN)	XP_024308866.1:p.Asp28998Val
XM_024453099.1:c.68756A>T (TTN)	XP_024308867.1:p.Asp22919Val
XM_024453100.1:c.58610A>T (TTN)	XP_024308868.1:p.Asp19537Val