Canonical Allele Identifier: CA1310548565

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178612477A= , CM000664.2:g.178612477A=	GRCh38
NC_000002.11:g.179477204A= , CM000664.1:g.179477204A=	GRCh37
NC_000002.10:g.179185449A=	NCBI36
NG_011618.3:g.223326T= , LRG_391:g.223326T=
NG_051363.1:g.94651A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.42344T= (TTN)	ENSP00000343764.6:p.Ile14115=
ENST00000342175.11:c.23429T= (TTN)	ENSP00000340554.6:p.Ile7810=
ENST00000359218.10:c.23228T= (TTN)	ENSP00000352154.5:p.Ile7743=
ENST00000342175.10:c.23429T= (TTN)	ENSP00000340554.6:p.Ile7810=
ENST00000342992.10:c.42344T= (TTN)	ENSP00000343764.6:p.Ile14115=
ENST00000359218.9:c.23228T= (TTN)	ENSP00000352154.5:p.Ile7743=
ENST00000460472.6:c.22853T= (TTN)	ENSP00000434586.1:p.Ile7618=
ENST00000589042.5:c.50048T= (TTN) MANE Select	ENSP00000467141.1:p.Ile16683=
ENST00000591111.5:c.45125T= (TTN)	ENSP00000465570.1:p.Ile15042=
ENST00000615779.4:c.45125T= (TTN)	ENSP00000483597.1:p.Ile15042=
NM_001256850.1:c.45125T= (TTN)	NP_001243779.1:p.Ile15042=
NM_001267550.2:c.50048T= (TTN) MANE Select	NP_001254479.2:p.Ile16683=
NM_003319.4:c.22853T= (TTN)	NP_003310.4:p.Ile7618=
NM_133378.4:c.42344T= (TTN)	NP_596869.4:p.Ile14115=
NM_133432.3:c.23228T= (TTN)	NP_597676.3:p.Ile7743=
NM_133437.4:c.23429T= (TTN)	NP_597681.4:p.Ile7810=
NR_038271.1:n.783-1558A= (TTN-AS1)
XM_011511729.1:c.49145T= (TTN)	XP_011510031.1:p.Ile16382=
XM_011511730.1:c.23039T= (TTN)	XP_011510032.1:p.Ile7680=
XM_011511731.1:c.22898T= (TTN)	XP_011510033.1:p.Ile7633=
XM_017004819.1:c.48941T= (TTN)	XP_016860308.1:p.Ile16314=
XM_017004820.1:c.44339T= (TTN)	XP_016860309.1:p.Ile14780=
XM_017004821.1:c.44336T= (TTN)	XP_016860310.1:p.Ile14779=
XM_017004822.1:c.41378T= (TTN)	XP_016860311.1:p.Ile13793=
XM_017004823.1:c.22994T= (TTN)	XP_016860312.1:p.Ile7665=
XM_024453094.1:c.44489T= (TTN)	XP_024308862.1:p.Ile14830=
XM_024453095.1:c.44486T= (TTN)	XP_024308863.1:p.Ile14829=
XM_024453096.1:c.43919T= (TTN)	XP_024308864.1:p.Ile14640=
XM_024453097.1:c.41261T= (TTN)	XP_024308865.1:p.Ile13754=
XM_024453098.1:c.41180T= (TTN)	XP_024308866.1:p.Ile13727=
XM_024453099.1:c.22943T= (TTN)	XP_024308867.1:p.Ile7648=
XM_024453100.1:c.12797T= (TTN)	XP_024308868.1:p.Ile4266=