Canonical Allele Identifier: CA1310522179

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552656T= , CM000664.2:g.178552656T=	GRCh38
NC_000002.11:g.179417383T= , CM000664.1:g.179417383T=	GRCh37
NC_000002.10:g.179125629T=	NCBI36
NG_011618.3:g.283147A= , LRG_391:g.283147A=
NG_051363.1:g.34830T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82540A= (TTN)	ENSP00000343764.6:p.Ile27514=
ENST00000342175.11:c.63625A= (TTN)	ENSP00000340554.6:p.Ile21209=
ENST00000359218.10:c.63424A= (TTN)	ENSP00000352154.5:p.Ile21142=
ENST00000342175.10:c.63625A= (TTN)	ENSP00000340554.6:p.Ile21209=
ENST00000342992.10:c.82540A= (TTN)	ENSP00000343764.6:p.Ile27514=
ENST00000359218.9:c.63424A= (TTN)	ENSP00000352154.5:p.Ile21142=
ENST00000460472.6:c.63049A= (TTN)	ENSP00000434586.1:p.Ile21017=
ENST00000589042.5:c.90244A= (TTN) MANE Select	ENSP00000467141.1:p.Ile30082=
ENST00000591111.5:c.85321A= (TTN)	ENSP00000465570.1:p.Ile28441=
ENST00000615779.4:c.85321A= (TTN)	ENSP00000483597.1:p.Ile28441=
NM_001256850.1:c.85321A= (TTN)	NP_001243779.1:p.Ile28441=
NM_001267550.2:c.90244A= (TTN) MANE Select	NP_001254479.2:p.Ile30082=
NM_003319.4:c.63049A= (TTN)	NP_003310.4:p.Ile21017=
NM_133378.4:c.82540A= (TTN)	NP_596869.4:p.Ile27514=
NM_133432.3:c.63424A= (TTN)	NP_597676.3:p.Ile21142=
NM_133437.4:c.63625A= (TTN)	NP_597681.4:p.Ile21209=
NR_038271.1:n.447-18644T= (TTN-AS1)
NR_038272.1:n.2043+10295T= (TTN-AS1)
XM_011511729.1:c.89341A= (TTN)	XP_011510031.1:p.Ile29781=
XM_011511730.1:c.63235A= (TTN)	XP_011510032.1:p.Ile21079=
XM_011511731.1:c.63094A= (TTN)	XP_011510033.1:p.Ile21032=
XM_017004819.1:c.89137A= (TTN)	XP_016860308.1:p.Ile29713=
XM_017004820.1:c.84535A= (TTN)	XP_016860309.1:p.Ile28179=
XM_017004821.1:c.84532A= (TTN)	XP_016860310.1:p.Ile28178=
XM_017004822.1:c.81574A= (TTN)	XP_016860311.1:p.Ile27192=
XM_017004823.1:c.63190A= (TTN)	XP_016860312.1:p.Ile21064=
XM_024453094.1:c.84685A= (TTN)	XP_024308862.1:p.Ile28229=
XM_024453095.1:c.84682A= (TTN)	XP_024308863.1:p.Ile28228=
XM_024453096.1:c.84115A= (TTN)	XP_024308864.1:p.Ile28039=
XM_024453097.1:c.81457A= (TTN)	XP_024308865.1:p.Ile27153=
XM_024453098.1:c.81376A= (TTN)	XP_024308866.1:p.Ile27126=
XM_024453099.1:c.63139A= (TTN)	XP_024308867.1:p.Ile21047=
XM_024453100.1:c.52993A= (TTN)	XP_024308868.1:p.Ile17665=