Canonical Allele Identifier: CA1310530958

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569092C= , CM000664.2:g.178569092C=	GRCh38
NC_000002.11:g.179433819C= , CM000664.1:g.179433819C=	GRCh37
NC_000002.10:g.179142065C=	NCBI36
NG_011618.3:g.266711G= , LRG_391:g.266711G=
NG_051363.1:g.51266C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.69336G= (TTN)	ENSP00000343764.6:p.Glu23112=
ENST00000342175.11:c.50421G= (TTN)	ENSP00000340554.6:p.Glu16807=
ENST00000359218.10:c.50220G= (TTN)	ENSP00000352154.5:p.Glu16740=
ENST00000342175.10:c.50421G= (TTN)	ENSP00000340554.6:p.Glu16807=
ENST00000342992.10:c.69336G= (TTN)	ENSP00000343764.6:p.Glu23112=
ENST00000359218.9:c.50220G= (TTN)	ENSP00000352154.5:p.Glu16740=
ENST00000460472.6:c.49845G= (TTN)	ENSP00000434586.1:p.Glu16615=
ENST00000589042.5:c.77040G= (TTN) MANE Select	ENSP00000467141.1:p.Glu25680=
ENST00000591111.5:c.72117G= (TTN)	ENSP00000465570.1:p.Glu24039=
ENST00000615779.4:c.72117G= (TTN)	ENSP00000483597.1:p.Glu24039=
NM_001256850.1:c.72117G= (TTN)	NP_001243779.1:p.Glu24039=
NM_001267550.2:c.77040G= (TTN) MANE Select	NP_001254479.2:p.Glu25680=
NM_003319.4:c.49845G= (TTN)	NP_003310.4:p.Glu16615=
NM_133378.4:c.69336G= (TTN)	NP_596869.4:p.Glu23112=
NM_133432.3:c.50220G= (TTN)	NP_597676.3:p.Glu16740=
NM_133437.4:c.50421G= (TTN)	NP_597681.4:p.Glu16807=
NR_038271.1:n.447-2208C= (TTN-AS1)
NR_038272.1:n.2044-13480C= (TTN-AS1)
XM_011511729.1:c.76137G= (TTN)	XP_011510031.1:p.Glu25379=
XM_011511730.1:c.50031G= (TTN)	XP_011510032.1:p.Glu16677=
XM_011511731.1:c.49890G= (TTN)	XP_011510033.1:p.Glu16630=
XM_017004819.1:c.75933G= (TTN)	XP_016860308.1:p.Glu25311=
XM_017004820.1:c.71331G= (TTN)	XP_016860309.1:p.Glu23777=
XM_017004821.1:c.71328G= (TTN)	XP_016860310.1:p.Glu23776=
XM_017004822.1:c.68370G= (TTN)	XP_016860311.1:p.Glu22790=
XM_017004823.1:c.49986G= (TTN)	XP_016860312.1:p.Glu16662=
XM_024453094.1:c.71481G= (TTN)	XP_024308862.1:p.Glu23827=
XM_024453095.1:c.71478G= (TTN)	XP_024308863.1:p.Glu23826=
XM_024453096.1:c.70911G= (TTN)	XP_024308864.1:p.Glu23637=
XM_024453097.1:c.68253G= (TTN)	XP_024308865.1:p.Glu22751=
XM_024453098.1:c.68172G= (TTN)	XP_024308866.1:p.Glu22724=
XM_024453099.1:c.49935G= (TTN)	XP_024308867.1:p.Glu16645=
XM_024453100.1:c.39789G= (TTN)	XP_024308868.1:p.Glu13263=