Canonical Allele Identifier: CA1310580094

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689136A= , CM000664.2:g.178689136A=	GRCh38
NC_000002.11:g.179553863A= , CM000664.1:g.179553863A=	GRCh37
NC_000002.10:g.179262108A=	NCBI36
NG_011618.3:g.146667T= , LRG_391:g.146667T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.28280T=	ENSP00000343764.6:p.Val9427=
ENST00000342175.11:c.13859-46819T=	ENSP00000340554.6:n.13859-46819T=
ENST00000359218.10:c.13658-46819T=	ENSP00000352154.5:n.13658-46819T=
ENST00000342175.10:c.13859-46819T=	ENSP00000340554.6:n.13859-46819T=
ENST00000342992.10:c.28280T=	ENSP00000343764.6:p.Val9427=
ENST00000359218.9:c.13658-46819T=	ENSP00000352154.5:n.13658-46819T=
ENST00000414766.5:c.1646T=	ENSP00000401501.1:p.Val549=
ENST00000460472.6:c.13283-46819T=	ENSP00000434586.1:n.13283-46819T=
ENST00000589042.5:c.32012T= MANE Select	ENSP00000467141.1:p.Val10671=
ENST00000591111.5:c.31061T=	ENSP00000465570.1:p.Val10354=
ENST00000615779.4:c.31061T=	ENSP00000483597.1:p.Val10354=
NM_001256850.1:c.31061T=	NP_001243779.1:p.Val10354=
NM_001267550.2:c.32012T= MANE Select	NP_001254479.2:p.Val10671=
NM_003319.4:c.13283-46819T=	NP_003310.4:n.13283-46819T=
NM_133378.4:c.28280T=	NP_596869.4:p.Val9427=
NM_133432.3:c.13658-46819T=	NP_597676.3:n.13658-46819T=
NM_133437.4:c.13859-46819T=	NP_597681.4:n.13859-46819T=
XM_011511729.1:c.31109T=	XP_011510031.1:p.Val10370=
XM_011511730.1:c.13469-46819T=	XP_011510032.1:n.13469-46819T=
XM_011511731.1:c.13328-46819T=	XP_011510033.1:n.13328-46819T=
XM_017004819.1:c.31064T=	XP_016860308.1:p.Val10355=
XM_017004820.1:c.28283T=	XP_016860309.1:p.Val9428=
XM_017004821.1:c.28280T=	XP_016860310.1:p.Val9427=
XM_017004822.1:c.31064T=	XP_016860311.1:p.Val10355=
XM_017004823.1:c.13424-46819T=	XP_016860312.1:n.13424-46819T=
XM_024453094.1:c.31064T=	XP_024308862.1:p.Val10355=
XM_024453095.1:c.31064T=	XP_024308863.1:p.Val10355=
XM_024453096.1:c.31064T=	XP_024308864.1:p.Val10355=
XM_024453097.1:c.30898+677T=	XP_024308865.1:n.30898+677T=
XM_024453098.1:c.30898+677T=	XP_024308866.1:n.30898+677T=
XM_024453099.1:c.13424-46819T=	XP_024308867.1:n.13424-46819T=