Canonical Allele Identifier: CA349504003

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179416562T>A (hg19) ; chr2:g.178551835T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551835T>A , CM000664.2:g.178551835T>A	GRCh38
NC_000002.11:g.179416562T>A , CM000664.1:g.179416562T>A	GRCh37
NC_000002.10:g.179124808T>A	NCBI36
NG_011618.3:g.283968A>T , LRG_391:g.283968A>T
NG_051363.1:g.34009T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.83361A>T (TTN)	ENSP00000343764.6:p.Glu27787Asp
ENST00000342175.11:c.64446A>T (TTN)	ENSP00000340554.6:p.Glu21482Asp
ENST00000359218.10:c.64245A>T (TTN)	ENSP00000352154.5:p.Glu21415Asp
ENST00000342175.10:c.64446A>T (TTN)	ENSP00000340554.6:p.Glu21482Asp
ENST00000342992.10:c.83361A>T (TTN)	ENSP00000343764.6:p.Glu27787Asp
ENST00000359218.9:c.64245A>T (TTN)	ENSP00000352154.5:p.Glu21415Asp
ENST00000460472.6:c.63870A>T (TTN)	ENSP00000434586.1:p.Glu21290Asp
ENST00000589042.5:c.91065A>T (TTN) MANE Select	ENSP00000467141.1:p.Glu30355Asp
ENST00000591111.5:c.86142A>T (TTN)	ENSP00000465570.1:p.Glu28714Asp
ENST00000615779.4:c.86142A>T (TTN)	ENSP00000483597.1:p.Glu28714Asp
NM_001256850.1:c.86142A>T (TTN)	NP_001243779.1:p.Glu28714Asp
NM_001267550.2:c.91065A>T (TTN) MANE Select	NP_001254479.2:p.Glu30355Asp
NM_003319.4:c.63870A>T (TTN)	NP_003310.4:p.Glu21290Asp
NM_133378.4:c.83361A>T (TTN)	NP_596869.4:p.Glu27787Asp
NM_133432.3:c.64245A>T (TTN)	NP_597676.3:p.Glu21415Asp
NM_133437.4:c.64446A>T (TTN)	NP_597681.4:p.Glu21482Asp
NR_038271.1:n.447-19465T>A (TTN-AS1)
NR_038272.1:n.2043+9474T>A (TTN-AS1)
XM_011511729.1:c.90162A>T (TTN)	XP_011510031.1:p.Glu30054Asp
XM_011511730.1:c.64056A>T (TTN)	XP_011510032.1:p.Glu21352Asp
XM_011511731.1:c.63915A>T (TTN)	XP_011510033.1:p.Glu21305Asp
XM_017004819.1:c.89958A>T (TTN)	XP_016860308.1:p.Glu29986Asp
XM_017004820.1:c.85356A>T (TTN)	XP_016860309.1:p.Glu28452Asp
XM_017004821.1:c.85353A>T (TTN)	XP_016860310.1:p.Glu28451Asp
XM_017004822.1:c.82395A>T (TTN)	XP_016860311.1:p.Glu27465Asp
XM_017004823.1:c.64011A>T (TTN)	XP_016860312.1:p.Glu21337Asp
XM_024453094.1:c.85506A>T (TTN)	XP_024308862.1:p.Glu28502Asp
XM_024453095.1:c.85503A>T (TTN)	XP_024308863.1:p.Glu28501Asp
XM_024453096.1:c.84936A>T (TTN)	XP_024308864.1:p.Glu28312Asp
XM_024453097.1:c.82278A>T (TTN)	XP_024308865.1:p.Glu27426Asp
XM_024453098.1:c.82197A>T (TTN)	XP_024308866.1:p.Glu27399Asp
XM_024453099.1:c.63960A>T (TTN)	XP_024308867.1:p.Glu21320Asp
XM_024453100.1:c.53814A>T (TTN)	XP_024308868.1:p.Glu17938Asp