Canonical Allele Identifier: CA349489034

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179413384T>C (hg19) ; chr2:g.178548657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178548657T>C , CM000664.2:g.178548657T>C	GRCh38
NC_000002.11:g.179413384T>C , CM000664.1:g.179413384T>C	GRCh37
NC_000002.10:g.179121630T>C	NCBI36
NG_011618.3:g.287146A>G , LRG_391:g.287146A>G
NG_051363.1:g.30831T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.85265A>G (TTN)	ENSP00000343764.6:p.Asp28422Gly
ENST00000342175.11:c.66350A>G (TTN)	ENSP00000340554.6:p.Asp22117Gly
ENST00000359218.10:c.66149A>G (TTN)	ENSP00000352154.5:p.Asp22050Gly
ENST00000342175.10:c.66350A>G (TTN)	ENSP00000340554.6:p.Asp22117Gly
ENST00000342992.10:c.85265A>G (TTN)	ENSP00000343764.6:p.Asp28422Gly
ENST00000359218.9:c.66149A>G (TTN)	ENSP00000352154.5:p.Asp22050Gly
ENST00000460472.6:c.65774A>G (TTN)	ENSP00000434586.1:p.Asp21925Gly
ENST00000589042.5:c.92969A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp30990Gly
ENST00000591111.5:c.88046A>G (TTN)	ENSP00000465570.1:p.Asp29349Gly
ENST00000615779.4:c.88046A>G (TTN)	ENSP00000483597.1:p.Asp29349Gly
NM_001256850.1:c.88046A>G (TTN)	NP_001243779.1:p.Asp29349Gly
NM_001267550.2:c.92969A>G (TTN) MANE Select	NP_001254479.2:p.Asp30990Gly
NM_003319.4:c.65774A>G (TTN)	NP_003310.4:p.Asp21925Gly
NM_133378.4:c.85265A>G (TTN)	NP_596869.4:p.Asp28422Gly
NM_133432.3:c.66149A>G (TTN)	NP_597676.3:p.Asp22050Gly
NM_133437.4:c.66350A>G (TTN)	NP_597681.4:p.Asp22117Gly
NR_038271.1:n.447-22643T>C (TTN-AS1)
NR_038272.1:n.2043+6296T>C (TTN-AS1)
XM_011511729.1:c.92066A>G (TTN)	XP_011510031.1:p.Asp30689Gly
XM_011511730.1:c.65960A>G (TTN)	XP_011510032.1:p.Asp21987Gly
XM_011511731.1:c.65819A>G (TTN)	XP_011510033.1:p.Asp21940Gly
XM_017004819.1:c.91862A>G (TTN)	XP_016860308.1:p.Asp30621Gly
XM_017004820.1:c.87260A>G (TTN)	XP_016860309.1:p.Asp29087Gly
XM_017004821.1:c.87257A>G (TTN)	XP_016860310.1:p.Asp29086Gly
XM_017004822.1:c.84299A>G (TTN)	XP_016860311.1:p.Asp28100Gly
XM_017004823.1:c.65915A>G (TTN)	XP_016860312.1:p.Asp21972Gly
XM_024453094.1:c.87410A>G (TTN)	XP_024308862.1:p.Asp29137Gly
XM_024453095.1:c.87407A>G (TTN)	XP_024308863.1:p.Asp29136Gly
XM_024453096.1:c.86840A>G (TTN)	XP_024308864.1:p.Asp28947Gly
XM_024453097.1:c.84182A>G (TTN)	XP_024308865.1:p.Asp28061Gly
XM_024453098.1:c.84101A>G (TTN)	XP_024308866.1:p.Asp28034Gly
XM_024453099.1:c.65864A>G (TTN)	XP_024308867.1:p.Asp21955Gly
XM_024453100.1:c.55718A>G (TTN)	XP_024308868.1:p.Asp18573Gly