Canonical Allele Identifier: CA1310600762

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178738159A= , CM000664.2:g.178738159A=	GRCh38
NC_000002.11:g.179602886A= , CM000664.1:g.179602886A=	GRCh37
NC_000002.10:g.179311131A=	NCBI36
NG_011618.3:g.97644T= , LRG_391:g.97644T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.10562T=	ENSP00000343764.6:p.Val3521=
ENST00000342175.11:c.13781T=	ENSP00000340554.6:p.Val4594=
ENST00000359218.10:c.13580T=	ENSP00000352154.5:p.Val4527=
ENST00000342175.10:c.13781T=	ENSP00000340554.6:p.Val4594=
ENST00000342992.10:c.10562T=	ENSP00000343764.6:p.Val3521=
ENST00000359218.9:c.13580T=	ENSP00000352154.5:p.Val4527=
ENST00000460472.6:c.13205T=	ENSP00000434586.1:p.Val4402=
ENST00000589042.5:c.14294T= MANE Select	ENSP00000467141.1:p.Val4765=
ENST00000591111.5:c.13343T=	ENSP00000465570.1:p.Val4448=
ENST00000615779.4:c.13343T=	ENSP00000483597.1:p.Val4448=
NM_001256850.1:c.13343T=	NP_001243779.1:p.Val4448=
NM_001267550.2:c.14294T= MANE Select	NP_001254479.2:p.Val4765=
NM_003319.4:c.13205T=	NP_003310.4:p.Val4402=
NM_133378.4:c.10562T=	NP_596869.4:p.Val3521=
NM_133432.3:c.13580T=	NP_597676.3:p.Val4527=
NM_133437.4:c.13781T=	NP_597681.4:p.Val4594=
XM_011511729.1:c.13391T=	XP_011510031.1:p.Val4464=
XM_011511730.1:c.13391T=	XP_011510032.1:p.Val4464=
XM_011511731.1:c.13250T=	XP_011510033.1:p.Val4417=
XM_017004819.1:c.13346T=	XP_016860308.1:p.Val4449=
XM_017004820.1:c.10565T=	XP_016860309.1:p.Val3522=
XM_017004821.1:c.10562T=	XP_016860310.1:p.Val3521=
XM_017004822.1:c.13346T=	XP_016860311.1:p.Val4449=
XM_017004823.1:c.13346T=	XP_016860312.1:p.Val4449=
XM_024453094.1:c.13346T=	XP_024308862.1:p.Val4449=
XM_024453095.1:c.13346T=	XP_024308863.1:p.Val4449=
XM_024453096.1:c.13346T=	XP_024308864.1:p.Val4449=
XM_024453097.1:c.13346T=	XP_024308865.1:p.Val4449=
XM_024453098.1:c.13346T=	XP_024308866.1:p.Val4449=
XM_024453099.1:c.13346T=	XP_024308867.1:p.Val4449=