Canonical Allele Identifier: CA1310549461

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614664C= , CM000664.2:g.178614664C=	GRCh38
NC_000002.11:g.179479391C= , CM000664.1:g.179479391C=	GRCh37
NC_000002.10:g.179187636C=	NCBI36
NG_011618.3:g.221139G= , LRG_391:g.221139G=
NG_051363.1:g.96838C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41146G= (TTN)	ENSP00000343764.6:p.Gly13716=
ENST00000342175.11:c.22231G= (TTN)	ENSP00000340554.6:p.Gly7411=
ENST00000359218.10:c.22030G= (TTN)	ENSP00000352154.5:p.Gly7344=
ENST00000342175.10:c.22231G= (TTN)	ENSP00000340554.6:p.Gly7411=
ENST00000342992.10:c.41146G= (TTN)	ENSP00000343764.6:p.Gly13716=
ENST00000359218.9:c.22030G= (TTN)	ENSP00000352154.5:p.Gly7344=
ENST00000460472.6:c.21655G= (TTN)	ENSP00000434586.1:p.Gly7219=
ENST00000589042.5:c.48850G= (TTN) MANE Select	ENSP00000467141.1:p.Gly16284=
ENST00000591111.5:c.43927G= (TTN)	ENSP00000465570.1:p.Gly14643=
ENST00000615779.4:c.43927G= (TTN)	ENSP00000483597.1:p.Gly14643=
NM_001256850.1:c.43927G= (TTN)	NP_001243779.1:p.Gly14643=
NM_001267550.2:c.48850G= (TTN) MANE Select	NP_001254479.2:p.Gly16284=
NM_003319.4:c.21655G= (TTN)	NP_003310.4:p.Gly7219=
NM_133378.4:c.41146G= (TTN)	NP_596869.4:p.Gly13716=
NM_133432.3:c.22030G= (TTN)	NP_597676.3:p.Gly7344=
NM_133437.4:c.22231G= (TTN)	NP_597681.4:p.Gly7411=
NR_038271.1:n.1412C= (TTN-AS1)
XM_011511729.1:c.47947G= (TTN)	XP_011510031.1:p.Gly15983=
XM_011511730.1:c.21841G= (TTN)	XP_011510032.1:p.Gly7281=
XM_011511731.1:c.21700G= (TTN)	XP_011510033.1:p.Gly7234=
XM_017004819.1:c.47743G= (TTN)	XP_016860308.1:p.Gly15915=
XM_017004820.1:c.43141G= (TTN)	XP_016860309.1:p.Gly14381=
XM_017004821.1:c.43138G= (TTN)	XP_016860310.1:p.Gly14380=
XM_017004822.1:c.40180G= (TTN)	XP_016860311.1:p.Gly13394=
XM_017004823.1:c.21796G= (TTN)	XP_016860312.1:p.Gly7266=
XM_024453094.1:c.43291G= (TTN)	XP_024308862.1:p.Gly14431=
XM_024453095.1:c.43288G= (TTN)	XP_024308863.1:p.Gly14430=
XM_024453096.1:c.42721G= (TTN)	XP_024308864.1:p.Gly14241=
XM_024453097.1:c.40063G= (TTN)	XP_024308865.1:p.Gly13355=
XM_024453098.1:c.39982G= (TTN)	XP_024308866.1:p.Gly13328=
XM_024453099.1:c.21745G= (TTN)	XP_024308867.1:p.Gly7249=
XM_024453100.1:c.11599G= (TTN)	XP_024308868.1:p.Gly3867=