Canonical Allele Identifier: CA1310522187

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552663G= , CM000664.2:g.178552663G=	GRCh38
NC_000002.11:g.179417390G= , CM000664.1:g.179417390G=	GRCh37
NC_000002.10:g.179125636G=	NCBI36
NG_011618.3:g.283140C= , LRG_391:g.283140C=
NG_051363.1:g.34837G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82533C= (TTN)	ENSP00000343764.6:p.His27511=
ENST00000342175.11:c.63618C= (TTN)	ENSP00000340554.6:p.His21206=
ENST00000359218.10:c.63417C= (TTN)	ENSP00000352154.5:p.His21139=
ENST00000342175.10:c.63618C= (TTN)	ENSP00000340554.6:p.His21206=
ENST00000342992.10:c.82533C= (TTN)	ENSP00000343764.6:p.His27511=
ENST00000359218.9:c.63417C= (TTN)	ENSP00000352154.5:p.His21139=
ENST00000460472.6:c.63042C= (TTN)	ENSP00000434586.1:p.His21014=
ENST00000589042.5:c.90237C= (TTN) MANE Select	ENSP00000467141.1:p.His30079=
ENST00000591111.5:c.85314C= (TTN)	ENSP00000465570.1:p.His28438=
ENST00000615779.4:c.85314C= (TTN)	ENSP00000483597.1:p.His28438=
NM_001256850.1:c.85314C= (TTN)	NP_001243779.1:p.His28438=
NM_001267550.2:c.90237C= (TTN) MANE Select	NP_001254479.2:p.His30079=
NM_003319.4:c.63042C= (TTN)	NP_003310.4:p.His21014=
NM_133378.4:c.82533C= (TTN)	NP_596869.4:p.His27511=
NM_133432.3:c.63417C= (TTN)	NP_597676.3:p.His21139=
NM_133437.4:c.63618C= (TTN)	NP_597681.4:p.His21206=
NR_038271.1:n.447-18637G= (TTN-AS1)
NR_038272.1:n.2043+10302G= (TTN-AS1)
XM_011511729.1:c.89334C= (TTN)	XP_011510031.1:p.His29778=
XM_011511730.1:c.63228C= (TTN)	XP_011510032.1:p.His21076=
XM_011511731.1:c.63087C= (TTN)	XP_011510033.1:p.His21029=
XM_017004819.1:c.89130C= (TTN)	XP_016860308.1:p.His29710=
XM_017004820.1:c.84528C= (TTN)	XP_016860309.1:p.His28176=
XM_017004821.1:c.84525C= (TTN)	XP_016860310.1:p.His28175=
XM_017004822.1:c.81567C= (TTN)	XP_016860311.1:p.His27189=
XM_017004823.1:c.63183C= (TTN)	XP_016860312.1:p.His21061=
XM_024453094.1:c.84678C= (TTN)	XP_024308862.1:p.His28226=
XM_024453095.1:c.84675C= (TTN)	XP_024308863.1:p.His28225=
XM_024453096.1:c.84108C= (TTN)	XP_024308864.1:p.His28036=
XM_024453097.1:c.81450C= (TTN)	XP_024308865.1:p.His27150=
XM_024453098.1:c.81369C= (TTN)	XP_024308866.1:p.His27123=
XM_024453099.1:c.63132C= (TTN)	XP_024308867.1:p.His21044=
XM_024453100.1:c.52986C= (TTN)	XP_024308868.1:p.His17662=