Canonical Allele Identifier: CA1310539828

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591112T= , CM000664.2:g.178591112T=	GRCh38
NC_000002.11:g.179455839T= , CM000664.1:g.179455839T=	GRCh37
NC_000002.10:g.179164085T=	NCBI36
NG_011618.3:g.244691A= , LRG_391:g.244691A=
NG_051363.1:g.73286T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52909A= (TTN)	ENSP00000343764.6:p.Ile17637=
ENST00000342175.11:c.33994A= (TTN)	ENSP00000340554.6:p.Ile11332=
ENST00000359218.10:c.33793A= (TTN)	ENSP00000352154.5:p.Ile11265=
ENST00000342175.10:c.33994A= (TTN)	ENSP00000340554.6:p.Ile11332=
ENST00000342992.10:c.52909A= (TTN)	ENSP00000343764.6:p.Ile17637=
ENST00000359218.9:c.33793A= (TTN)	ENSP00000352154.5:p.Ile11265=
ENST00000460472.6:c.33418A= (TTN)	ENSP00000434586.1:p.Ile11140=
ENST00000589042.5:c.60613A= (TTN) MANE Select	ENSP00000467141.1:p.Ile20205=
ENST00000591111.5:c.55690A= (TTN)	ENSP00000465570.1:p.Ile18564=
ENST00000615779.4:c.55690A= (TTN)	ENSP00000483597.1:p.Ile18564=
NM_001256850.1:c.55690A= (TTN)	NP_001243779.1:p.Ile18564=
NM_001267550.2:c.60613A= (TTN) MANE Select	NP_001254479.2:p.Ile20205=
NM_003319.4:c.33418A= (TTN)	NP_003310.4:p.Ile11140=
NM_133378.4:c.52909A= (TTN)	NP_596869.4:p.Ile17637=
NM_133432.3:c.33793A= (TTN)	NP_597676.3:p.Ile11265=
NM_133437.4:c.33994A= (TTN)	NP_597681.4:p.Ile11332=
NR_038271.1:n.597-6484T= (TTN-AS1)
NR_038272.1:n.3189-27T= (TTN-AS1)
XM_011511729.1:c.59710A= (TTN)	XP_011510031.1:p.Ile19904=
XM_011511730.1:c.33604A= (TTN)	XP_011510032.1:p.Ile11202=
XM_011511731.1:c.33463A= (TTN)	XP_011510033.1:p.Ile11155=
XM_017004819.1:c.59506A= (TTN)	XP_016860308.1:p.Ile19836=
XM_017004820.1:c.54904A= (TTN)	XP_016860309.1:p.Ile18302=
XM_017004821.1:c.54901A= (TTN)	XP_016860310.1:p.Ile18301=
XM_017004822.1:c.51943A= (TTN)	XP_016860311.1:p.Ile17315=
XM_017004823.1:c.33559A= (TTN)	XP_016860312.1:p.Ile11187=
XM_024453094.1:c.55054A= (TTN)	XP_024308862.1:p.Ile18352=
XM_024453095.1:c.55051A= (TTN)	XP_024308863.1:p.Ile18351=
XM_024453096.1:c.54484A= (TTN)	XP_024308864.1:p.Ile18162=
XM_024453097.1:c.51826A= (TTN)	XP_024308865.1:p.Ile17276=
XM_024453098.1:c.51745A= (TTN)	XP_024308866.1:p.Ile17249=
XM_024453099.1:c.33508A= (TTN)	XP_024308867.1:p.Ile11170=
XM_024453100.1:c.23362A= (TTN)	XP_024308868.1:p.Ile7788=