Canonical Allele Identifier: CA1310514588

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530398C= , CM000664.2:g.178530398C=	GRCh38
NC_000002.11:g.179395125C= , CM000664.1:g.179395125C=	GRCh37
NC_000002.10:g.179103371C=	NCBI36
NG_011618.3:g.305405G= , LRG_391:g.305405G=
NG_051363.1:g.12572C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.98513G= (TTN)	ENSP00000343764.6:p.Arg32838=
ENST00000342175.11:c.79598G= (TTN)	ENSP00000340554.6:p.Arg26533=
ENST00000359218.10:c.79397G= (TTN)	ENSP00000352154.5:p.Arg26466=
ENST00000342175.10:c.79598G= (TTN)	ENSP00000340554.6:p.Arg26533=
ENST00000342992.10:c.98513G= (TTN)	ENSP00000343764.6:p.Arg32838=
ENST00000359218.9:c.79397G= (TTN)	ENSP00000352154.5:p.Arg26466=
ENST00000460472.6:c.79022G= (TTN)	ENSP00000434586.1:p.Arg26341=
ENST00000589042.5:c.106217G= (TTN) MANE Select	ENSP00000467141.1:p.Arg35406=
ENST00000591111.5:c.101294G= (TTN)	ENSP00000465570.1:p.Arg33765=
ENST00000615779.4:c.101294G= (TTN)	ENSP00000483597.1:p.Arg33765=
NM_001256850.1:c.101294G= (TTN)	NP_001243779.1:p.Arg33765=
NM_001267550.2:c.106217G= (TTN) MANE Select	NP_001254479.2:p.Arg35406=
NM_003319.4:c.79022G= (TTN)	NP_003310.4:p.Arg26341=
NM_133378.4:c.98513G= (TTN)	NP_596869.4:p.Arg32838=
NM_133432.3:c.79397G= (TTN)	NP_597676.3:p.Arg26466=
NM_133437.4:c.79598G= (TTN)	NP_597681.4:p.Arg26533=
NR_038271.1:n.446+6762C= (TTN-AS1)
NR_038272.1:n.220-5334C= (TTN-AS1)
XM_011511729.1:c.105314G= (TTN)	XP_011510031.1:p.Arg35105=
XM_011511730.1:c.79208G= (TTN)	XP_011510032.1:p.Arg26403=
XM_011511731.1:c.79067G= (TTN)	XP_011510033.1:p.Arg26356=
XM_017004819.1:c.105110G= (TTN)	XP_016860308.1:p.Arg35037=
XM_017004820.1:c.100508G= (TTN)	XP_016860309.1:p.Arg33503=
XM_017004821.1:c.100505G= (TTN)	XP_016860310.1:p.Arg33502=
XM_017004822.1:c.97547G= (TTN)	XP_016860311.1:p.Arg32516=
XM_017004823.1:c.79163G= (TTN)	XP_016860312.1:p.Arg26388=
XM_024453094.1:c.100658G= (TTN)	XP_024308862.1:p.Arg33553=
XM_024453095.1:c.100655G= (TTN)	XP_024308863.1:p.Arg33552=
XM_024453096.1:c.100088G= (TTN)	XP_024308864.1:p.Arg33363=
XM_024453097.1:c.97430G= (TTN)	XP_024308865.1:p.Arg32477=
XM_024453098.1:c.97349G= (TTN)	XP_024308866.1:p.Arg32450=
XM_024453099.1:c.79112G= (TTN)	XP_024308867.1:p.Arg26371=
XM_024453100.1:c.68966G= (TTN)	XP_024308868.1:p.Arg22989=