Canonical Allele Identifier: CA1310600760

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178738156T= , CM000664.2:g.178738156T=	GRCh38
NC_000002.11:g.179602883T= , CM000664.1:g.179602883T=	GRCh37
NC_000002.10:g.179311128T=	NCBI36
NG_011618.3:g.97647A= , LRG_391:g.97647A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.10565A=	ENSP00000343764.6:p.Asp3522=
ENST00000342175.11:c.13784A=	ENSP00000340554.6:p.Asp4595=
ENST00000359218.10:c.13583A=	ENSP00000352154.5:p.Asp4528=
ENST00000342175.10:c.13784A=	ENSP00000340554.6:p.Asp4595=
ENST00000342992.10:c.10565A=	ENSP00000343764.6:p.Asp3522=
ENST00000359218.9:c.13583A=	ENSP00000352154.5:p.Asp4528=
ENST00000460472.6:c.13208A=	ENSP00000434586.1:p.Asp4403=
ENST00000589042.5:c.14297A= MANE Select	ENSP00000467141.1:p.Asp4766=
ENST00000591111.5:c.13346A=	ENSP00000465570.1:p.Asp4449=
ENST00000615779.4:c.13346A=	ENSP00000483597.1:p.Asp4449=
NM_001256850.1:c.13346A=	NP_001243779.1:p.Asp4449=
NM_001267550.2:c.14297A= MANE Select	NP_001254479.2:p.Asp4766=
NM_003319.4:c.13208A=	NP_003310.4:p.Asp4403=
NM_133378.4:c.10565A=	NP_596869.4:p.Asp3522=
NM_133432.3:c.13583A=	NP_597676.3:p.Asp4528=
NM_133437.4:c.13784A=	NP_597681.4:p.Asp4595=
XM_011511729.1:c.13394A=	XP_011510031.1:p.Asp4465=
XM_011511730.1:c.13394A=	XP_011510032.1:p.Asp4465=
XM_011511731.1:c.13253A=	XP_011510033.1:p.Asp4418=
XM_017004819.1:c.13349A=	XP_016860308.1:p.Asp4450=
XM_017004820.1:c.10568A=	XP_016860309.1:p.Asp3523=
XM_017004821.1:c.10565A=	XP_016860310.1:p.Asp3522=
XM_017004822.1:c.13349A=	XP_016860311.1:p.Asp4450=
XM_017004823.1:c.13349A=	XP_016860312.1:p.Asp4450=
XM_024453094.1:c.13349A=	XP_024308862.1:p.Asp4450=
XM_024453095.1:c.13349A=	XP_024308863.1:p.Asp4450=
XM_024453096.1:c.13349A=	XP_024308864.1:p.Asp4450=
XM_024453097.1:c.13349A=	XP_024308865.1:p.Asp4450=
XM_024453098.1:c.13349A=	XP_024308866.1:p.Asp4450=
XM_024453099.1:c.13349A=	XP_024308867.1:p.Asp4450=