Canonical Allele Identifier: CA349450628

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408597C>A (hg19) ; chr2:g.178543870C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543870C>A , CM000664.2:g.178543870C>A	GRCh38
NC_000002.11:g.179408597C>A , CM000664.1:g.179408597C>A	GRCh37
NC_000002.10:g.179116843C>A	NCBI36
NG_011618.3:g.291933G>T , LRG_391:g.291933G>T
NG_051363.1:g.26044C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88570G>T (TTN)	ENSP00000343764.6:p.Gly29524Cys
ENST00000342175.11:c.69655G>T (TTN)	ENSP00000340554.6:p.Gly23219Cys
ENST00000359218.10:c.69454G>T (TTN)	ENSP00000352154.5:p.Gly23152Cys
ENST00000342175.10:c.69655G>T (TTN)	ENSP00000340554.6:p.Gly23219Cys
ENST00000342992.10:c.88570G>T (TTN)	ENSP00000343764.6:p.Gly29524Cys
ENST00000359218.9:c.69454G>T (TTN)	ENSP00000352154.5:p.Gly23152Cys
ENST00000460472.6:c.69079G>T (TTN)	ENSP00000434586.1:p.Gly23027Cys
ENST00000589042.5:c.96274G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly32092Cys
ENST00000591111.5:c.91351G>T (TTN)	ENSP00000465570.1:p.Gly30451Cys
ENST00000615779.4:c.91351G>T (TTN)	ENSP00000483597.1:p.Gly30451Cys
NM_001256850.1:c.91351G>T (TTN)	NP_001243779.1:p.Gly30451Cys
NM_001267550.2:c.96274G>T (TTN) MANE Select	NP_001254479.2:p.Gly32092Cys
NM_003319.4:c.69079G>T (TTN)	NP_003310.4:p.Gly23027Cys
NM_133378.4:c.88570G>T (TTN)	NP_596869.4:p.Gly29524Cys
NM_133432.3:c.69454G>T (TTN)	NP_597676.3:p.Gly23152Cys
NM_133437.4:c.69655G>T (TTN)	NP_597681.4:p.Gly23219Cys
NR_038271.1:n.446+20234C>A (TTN-AS1)
NR_038272.1:n.2043+1509C>A (TTN-AS1)
XM_011511729.1:c.95371G>T (TTN)	XP_011510031.1:p.Gly31791Cys
XM_011511730.1:c.69265G>T (TTN)	XP_011510032.1:p.Gly23089Cys
XM_011511731.1:c.69124G>T (TTN)	XP_011510033.1:p.Gly23042Cys
XM_017004819.1:c.95167G>T (TTN)	XP_016860308.1:p.Gly31723Cys
XM_017004820.1:c.90565G>T (TTN)	XP_016860309.1:p.Gly30189Cys
XM_017004821.1:c.90562G>T (TTN)	XP_016860310.1:p.Gly30188Cys
XM_017004822.1:c.87604G>T (TTN)	XP_016860311.1:p.Gly29202Cys
XM_017004823.1:c.69220G>T (TTN)	XP_016860312.1:p.Gly23074Cys
XM_024453094.1:c.90715G>T (TTN)	XP_024308862.1:p.Gly30239Cys
XM_024453095.1:c.90712G>T (TTN)	XP_024308863.1:p.Gly30238Cys
XM_024453096.1:c.90145G>T (TTN)	XP_024308864.1:p.Gly30049Cys
XM_024453097.1:c.87487G>T (TTN)	XP_024308865.1:p.Gly29163Cys
XM_024453098.1:c.87406G>T (TTN)	XP_024308866.1:p.Gly29136Cys
XM_024453099.1:c.69169G>T (TTN)	XP_024308867.1:p.Gly23057Cys
XM_024453100.1:c.59023G>T (TTN)	XP_024308868.1:p.Gly19675Cys