Canonical Allele Identifier: CA1310530790

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569888A= , CM000664.2:g.178569888A=	GRCh38
NC_000002.11:g.179434615A= , CM000664.1:g.179434615A=	GRCh37
NC_000002.10:g.179142861A=	NCBI36
NG_011618.3:g.265915T= , LRG_391:g.265915T=
NG_051363.1:g.52062A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.68540T= (TTN)	ENSP00000343764.6:p.Ile22847=
ENST00000342175.11:c.49625T= (TTN)	ENSP00000340554.6:p.Ile16542=
ENST00000359218.10:c.49424T= (TTN)	ENSP00000352154.5:p.Ile16475=
ENST00000342175.10:c.49625T= (TTN)	ENSP00000340554.6:p.Ile16542=
ENST00000342992.10:c.68540T= (TTN)	ENSP00000343764.6:p.Ile22847=
ENST00000359218.9:c.49424T= (TTN)	ENSP00000352154.5:p.Ile16475=
ENST00000460472.6:c.49049T= (TTN)	ENSP00000434586.1:p.Ile16350=
ENST00000589042.5:c.76244T= (TTN) MANE Select	ENSP00000467141.1:p.Ile25415=
ENST00000591111.5:c.71321T= (TTN)	ENSP00000465570.1:p.Ile23774=
ENST00000615779.4:c.71321T= (TTN)	ENSP00000483597.1:p.Ile23774=
NM_001256850.1:c.71321T= (TTN)	NP_001243779.1:p.Ile23774=
NM_001267550.2:c.76244T= (TTN) MANE Select	NP_001254479.2:p.Ile25415=
NM_003319.4:c.49049T= (TTN)	NP_003310.4:p.Ile16350=
NM_133378.4:c.68540T= (TTN)	NP_596869.4:p.Ile22847=
NM_133432.3:c.49424T= (TTN)	NP_597676.3:p.Ile16475=
NM_133437.4:c.49625T= (TTN)	NP_597681.4:p.Ile16542=
NR_038271.1:n.447-1412A= (TTN-AS1)
NR_038272.1:n.2044-12684A= (TTN-AS1)
XM_011511729.1:c.75341T= (TTN)	XP_011510031.1:p.Ile25114=
XM_011511730.1:c.49235T= (TTN)	XP_011510032.1:p.Ile16412=
XM_011511731.1:c.49094T= (TTN)	XP_011510033.1:p.Ile16365=
XM_017004819.1:c.75137T= (TTN)	XP_016860308.1:p.Ile25046=
XM_017004820.1:c.70535T= (TTN)	XP_016860309.1:p.Ile23512=
XM_017004821.1:c.70532T= (TTN)	XP_016860310.1:p.Ile23511=
XM_017004822.1:c.67574T= (TTN)	XP_016860311.1:p.Ile22525=
XM_017004823.1:c.49190T= (TTN)	XP_016860312.1:p.Ile16397=
XM_024453094.1:c.70685T= (TTN)	XP_024308862.1:p.Ile23562=
XM_024453095.1:c.70682T= (TTN)	XP_024308863.1:p.Ile23561=
XM_024453096.1:c.70115T= (TTN)	XP_024308864.1:p.Ile23372=
XM_024453097.1:c.67457T= (TTN)	XP_024308865.1:p.Ile22486=
XM_024453098.1:c.67376T= (TTN)	XP_024308866.1:p.Ile22459=
XM_024453099.1:c.49139T= (TTN)	XP_024308867.1:p.Ile16380=
XM_024453100.1:c.38993T= (TTN)	XP_024308868.1:p.Ile12998=