Canonical Allele Identifier: CA349618202

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179482785C>A (hg19) ; chr2:g.178618058C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618058C>A , CM000664.2:g.178618058C>A	GRCh38
NC_000002.11:g.179482785C>A , CM000664.1:g.179482785C>A	GRCh37
NC_000002.10:g.179191030C>A	NCBI36
NG_011618.3:g.217745G>T , LRG_391:g.217745G>T
NG_051363.1:g.100232C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.39589G>T (TTN)	ENSP00000343764.6:p.Val13197Leu
ENST00000342175.11:c.20674G>T (TTN)	ENSP00000340554.6:p.Val6892Leu
ENST00000359218.10:c.20473G>T (TTN)	ENSP00000352154.5:p.Val6825Leu
ENST00000342175.10:c.20674G>T (TTN)	ENSP00000340554.6:p.Val6892Leu
ENST00000342992.10:c.39589G>T (TTN)	ENSP00000343764.6:p.Val13197Leu
ENST00000359218.9:c.20473G>T (TTN)	ENSP00000352154.5:p.Val6825Leu
ENST00000460472.6:c.20098G>T (TTN)	ENSP00000434586.1:p.Val6700Leu
ENST00000589042.5:c.47293G>T (TTN) MANE Select	ENSP00000467141.1:p.Val15765Leu
ENST00000591111.5:c.42370G>T (TTN)	ENSP00000465570.1:p.Val14124Leu
ENST00000615779.4:c.42370G>T (TTN)	ENSP00000483597.1:p.Val14124Leu
NM_001256850.1:c.42370G>T (TTN)	NP_001243779.1:p.Val14124Leu
NM_001267550.2:c.47293G>T (TTN) MANE Select	NP_001254479.2:p.Val15765Leu
NM_003319.4:c.20098G>T (TTN)	NP_003310.4:p.Val6700Leu
NM_133378.4:c.39589G>T (TTN)	NP_596869.4:p.Val13197Leu
NM_133432.3:c.20473G>T (TTN)	NP_597676.3:p.Val6825Leu
NM_133437.4:c.20674G>T (TTN)	NP_597681.4:p.Val6892Leu
NR_038271.1:n.1605-1695C>A (TTN-AS1)
XM_011511729.1:c.46390G>T (TTN)	XP_011510031.1:p.Val15464Leu
XM_011511730.1:c.20284G>T (TTN)	XP_011510032.1:p.Val6762Leu
XM_011511731.1:c.20143G>T (TTN)	XP_011510033.1:p.Val6715Leu
XM_017004819.1:c.46186G>T (TTN)	XP_016860308.1:p.Val15396Leu
XM_017004820.1:c.41584G>T (TTN)	XP_016860309.1:p.Val13862Leu
XM_017004821.1:c.41581G>T (TTN)	XP_016860310.1:p.Val13861Leu
XM_017004822.1:c.38623G>T (TTN)	XP_016860311.1:p.Val12875Leu
XM_017004823.1:c.20239G>T (TTN)	XP_016860312.1:p.Val6747Leu
XM_024453094.1:c.41734G>T (TTN)	XP_024308862.1:p.Val13912Leu
XM_024453095.1:c.41731G>T (TTN)	XP_024308863.1:p.Val13911Leu
XM_024453096.1:c.41164G>T (TTN)	XP_024308864.1:p.Val13722Leu
XM_024453097.1:c.38506G>T (TTN)	XP_024308865.1:p.Val12836Leu
XM_024453098.1:c.38425G>T (TTN)	XP_024308866.1:p.Val12809Leu
XM_024453099.1:c.20188G>T (TTN)	XP_024308867.1:p.Val6730Leu
XM_024453100.1:c.10042G>T (TTN)	XP_024308868.1:p.Val3348Leu