Canonical Allele Identifier: CA1310529057

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178565416G= , CM000664.2:g.178565416G=	GRCh38
NC_000002.11:g.179430143G= , CM000664.1:g.179430143G=	GRCh37
NC_000002.10:g.179138389G=	NCBI36
NG_011618.3:g.270387C= , LRG_391:g.270387C=
NG_051363.1:g.47590G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.73012C= (TTN)	ENSP00000343764.6:p.Arg24338=
ENST00000342175.11:c.54097C= (TTN)	ENSP00000340554.6:p.Arg18033=
ENST00000359218.10:c.53896C= (TTN)	ENSP00000352154.5:p.Arg17966=
ENST00000342175.10:c.54097C= (TTN)	ENSP00000340554.6:p.Arg18033=
ENST00000342992.10:c.73012C= (TTN)	ENSP00000343764.6:p.Arg24338=
ENST00000359218.9:c.53896C= (TTN)	ENSP00000352154.5:p.Arg17966=
ENST00000460472.6:c.53521C= (TTN)	ENSP00000434586.1:p.Arg17841=
ENST00000589042.5:c.80716C= (TTN) MANE Select	ENSP00000467141.1:p.Arg26906=
ENST00000591111.5:c.75793C= (TTN)	ENSP00000465570.1:p.Arg25265=
ENST00000615779.4:c.75793C= (TTN)	ENSP00000483597.1:p.Arg25265=
NM_001256850.1:c.75793C= (TTN)	NP_001243779.1:p.Arg25265=
NM_001267550.2:c.80716C= (TTN) MANE Select	NP_001254479.2:p.Arg26906=
NM_003319.4:c.53521C= (TTN)	NP_003310.4:p.Arg17841=
NM_133378.4:c.73012C= (TTN)	NP_596869.4:p.Arg24338=
NM_133432.3:c.53896C= (TTN)	NP_597676.3:p.Arg17966=
NM_133437.4:c.54097C= (TTN)	NP_597681.4:p.Arg18033=
NR_038271.1:n.447-5884G= (TTN-AS1)
NR_038272.1:n.2044-17156G= (TTN-AS1)
XM_011511729.1:c.79813C= (TTN)	XP_011510031.1:p.Arg26605=
XM_011511730.1:c.53707C= (TTN)	XP_011510032.1:p.Arg17903=
XM_011511731.1:c.53566C= (TTN)	XP_011510033.1:p.Arg17856=
XM_017004819.1:c.79609C= (TTN)	XP_016860308.1:p.Arg26537=
XM_017004820.1:c.75007C= (TTN)	XP_016860309.1:p.Arg25003=
XM_017004821.1:c.75004C= (TTN)	XP_016860310.1:p.Arg25002=
XM_017004822.1:c.72046C= (TTN)	XP_016860311.1:p.Arg24016=
XM_017004823.1:c.53662C= (TTN)	XP_016860312.1:p.Arg17888=
XM_024453094.1:c.75157C= (TTN)	XP_024308862.1:p.Arg25053=
XM_024453095.1:c.75154C= (TTN)	XP_024308863.1:p.Arg25052=
XM_024453096.1:c.74587C= (TTN)	XP_024308864.1:p.Arg24863=
XM_024453097.1:c.71929C= (TTN)	XP_024308865.1:p.Arg23977=
XM_024453098.1:c.71848C= (TTN)	XP_024308866.1:p.Arg23950=
XM_024453099.1:c.53611C= (TTN)	XP_024308867.1:p.Arg17871=
XM_024453100.1:c.43465C= (TTN)	XP_024308868.1:p.Arg14489=