Canonical Allele Identifier: CA349494148

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179457504A>T (hg19) ; chr2:g.178592777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178592777A>T , CM000664.2:g.178592777A>T	GRCh38
NC_000002.11:g.179457504A>T , CM000664.1:g.179457504A>T	GRCh37
NC_000002.10:g.179165750A>T	NCBI36
NG_011618.3:g.243026T>A , LRG_391:g.243026T>A
NG_051363.1:g.74951A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.51638T>A (TTN)	ENSP00000343764.6:p.Leu17213His
ENST00000342175.11:c.32723T>A (TTN)	ENSP00000340554.6:p.Leu10908His
ENST00000359218.10:c.32522T>A (TTN)	ENSP00000352154.5:p.Leu10841His
ENST00000342175.10:c.32723T>A (TTN)	ENSP00000340554.6:p.Leu10908His
ENST00000342992.10:c.51638T>A (TTN)	ENSP00000343764.6:p.Leu17213His
ENST00000359218.9:c.32522T>A (TTN)	ENSP00000352154.5:p.Leu10841His
ENST00000460472.6:c.32147T>A (TTN)	ENSP00000434586.1:p.Leu10716His
ENST00000589042.5:c.59342T>A (TTN) MANE Select	ENSP00000467141.1:p.Leu19781His
ENST00000591111.5:c.54419T>A (TTN)	ENSP00000465570.1:p.Leu18140His
ENST00000615779.4:c.54419T>A (TTN)	ENSP00000483597.1:p.Leu18140His
NM_001256850.1:c.54419T>A (TTN)	NP_001243779.1:p.Leu18140His
NM_001267550.2:c.59342T>A (TTN) MANE Select	NP_001254479.2:p.Leu19781His
NM_003319.4:c.32147T>A (TTN)	NP_003310.4:p.Leu10716His
NM_133378.4:c.51638T>A (TTN)	NP_596869.4:p.Leu17213His
NM_133432.3:c.32522T>A (TTN)	NP_597676.3:p.Leu10841His
NM_133437.4:c.32723T>A (TTN)	NP_597681.4:p.Leu10908His
NR_038271.1:n.597-4819A>T (TTN-AS1)
NR_038272.1:n.3364+1463A>T (TTN-AS1)
XM_011511729.1:c.58439T>A (TTN)	XP_011510031.1:p.Leu19480His
XM_011511730.1:c.32333T>A (TTN)	XP_011510032.1:p.Leu10778His
XM_011511731.1:c.32192T>A (TTN)	XP_011510033.1:p.Leu10731His
XM_017004819.1:c.58235T>A (TTN)	XP_016860308.1:p.Leu19412His
XM_017004820.1:c.53633T>A (TTN)	XP_016860309.1:p.Leu17878His
XM_017004821.1:c.53630T>A (TTN)	XP_016860310.1:p.Leu17877His
XM_017004822.1:c.50672T>A (TTN)	XP_016860311.1:p.Leu16891His
XM_017004823.1:c.32288T>A (TTN)	XP_016860312.1:p.Leu10763His
XM_024453094.1:c.53783T>A (TTN)	XP_024308862.1:p.Leu17928His
XM_024453095.1:c.53780T>A (TTN)	XP_024308863.1:p.Leu17927His
XM_024453096.1:c.53213T>A (TTN)	XP_024308864.1:p.Leu17738His
XM_024453097.1:c.50555T>A (TTN)	XP_024308865.1:p.Leu16852His
XM_024453098.1:c.50474T>A (TTN)	XP_024308866.1:p.Leu16825His
XM_024453099.1:c.32237T>A (TTN)	XP_024308867.1:p.Leu10746His
XM_024453100.1:c.22091T>A (TTN)	XP_024308868.1:p.Leu7364His