Canonical Allele Identifier: CA349407135

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395289T>G (hg19) ; chr2:g.178530562T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530562T>G , CM000664.2:g.178530562T>G	GRCh38
NC_000002.11:g.179395289T>G , CM000664.1:g.179395289T>G	GRCh37
NC_000002.10:g.179103535T>G	NCBI36
NG_011618.3:g.305241A>C , LRG_391:g.305241A>C
NG_051363.1:g.12736T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98349A>C (TTN)	ENSP00000343764.6:p.Glu32783Asp
ENST00000342175.11:c.79434A>C (TTN)	ENSP00000340554.6:p.Glu26478Asp
ENST00000359218.10:c.79233A>C (TTN)	ENSP00000352154.5:p.Glu26411Asp
ENST00000342175.10:c.79434A>C (TTN)	ENSP00000340554.6:p.Glu26478Asp
ENST00000342992.10:c.98349A>C (TTN)	ENSP00000343764.6:p.Glu32783Asp
ENST00000359218.9:c.79233A>C (TTN)	ENSP00000352154.5:p.Glu26411Asp
ENST00000460472.6:c.78858A>C (TTN)	ENSP00000434586.1:p.Glu26286Asp
ENST00000589042.5:c.106053A>C (TTN) MANE Select	ENSP00000467141.1:p.Glu35351Asp
ENST00000591111.5:c.101130A>C (TTN)	ENSP00000465570.1:p.Glu33710Asp
ENST00000615779.4:c.101130A>C (TTN)	ENSP00000483597.1:p.Glu33710Asp
NM_001256850.1:c.101130A>C (TTN)	NP_001243779.1:p.Glu33710Asp
NM_001267550.2:c.106053A>C (TTN) MANE Select	NP_001254479.2:p.Glu35351Asp
NM_003319.4:c.78858A>C (TTN)	NP_003310.4:p.Glu26286Asp
NM_133378.4:c.98349A>C (TTN)	NP_596869.4:p.Glu32783Asp
NM_133432.3:c.79233A>C (TTN)	NP_597676.3:p.Glu26411Asp
NM_133437.4:c.79434A>C (TTN)	NP_597681.4:p.Glu26478Asp
NR_038271.1:n.446+6926T>G (TTN-AS1)
NR_038272.1:n.220-5170T>G (TTN-AS1)
XM_011511729.1:c.105150A>C (TTN)	XP_011510031.1:p.Glu35050Asp
XM_011511730.1:c.79044A>C (TTN)	XP_011510032.1:p.Glu26348Asp
XM_011511731.1:c.78903A>C (TTN)	XP_011510033.1:p.Glu26301Asp
XM_017004819.1:c.104946A>C (TTN)	XP_016860308.1:p.Glu34982Asp
XM_017004820.1:c.100344A>C (TTN)	XP_016860309.1:p.Glu33448Asp
XM_017004821.1:c.100341A>C (TTN)	XP_016860310.1:p.Glu33447Asp
XM_017004822.1:c.97383A>C (TTN)	XP_016860311.1:p.Glu32461Asp
XM_017004823.1:c.78999A>C (TTN)	XP_016860312.1:p.Glu26333Asp
XM_024453094.1:c.100494A>C (TTN)	XP_024308862.1:p.Glu33498Asp
XM_024453095.1:c.100491A>C (TTN)	XP_024308863.1:p.Glu33497Asp
XM_024453096.1:c.99924A>C (TTN)	XP_024308864.1:p.Glu33308Asp
XM_024453097.1:c.97266A>C (TTN)	XP_024308865.1:p.Glu32422Asp
XM_024453098.1:c.97185A>C (TTN)	XP_024308866.1:p.Glu32395Asp
XM_024453099.1:c.78948A>C (TTN)	XP_024308867.1:p.Glu26316Asp
XM_024453100.1:c.68802A>C (TTN)	XP_024308868.1:p.Glu22934Asp