Canonical Allele Identifier: CA1310555933

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630336T= , CM000664.2:g.178630336T=	GRCh38
NC_000002.11:g.179495063T= , CM000664.1:g.179495063T=	GRCh37
NC_000002.10:g.179203308T=	NCBI36
NG_011618.3:g.205467A= , LRG_391:g.205467A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.36482A=	ENSP00000343764.6:p.His12161=
ENST00000342175.11:c.17567A=	ENSP00000340554.6:p.His5856=
ENST00000359218.10:c.17366A=	ENSP00000352154.5:p.His5789=
ENST00000342175.10:c.17567A=	ENSP00000340554.6:p.His5856=
ENST00000342992.10:c.36482A=	ENSP00000343764.6:p.His12161=
ENST00000359218.9:c.17366A=	ENSP00000352154.5:p.His5789=
ENST00000460472.6:c.16991A=	ENSP00000434586.1:p.His5664=
ENST00000589042.5:c.44186A= MANE Select	ENSP00000467141.1:p.His14729=
ENST00000591111.5:c.39263A=	ENSP00000465570.1:p.His13088=
ENST00000615779.4:c.39263A=	ENSP00000483597.1:p.His13088=
NM_001256850.1:c.39263A=	NP_001243779.1:p.His13088=
NM_001267550.2:c.44186A= MANE Select	NP_001254479.2:p.His14729=
NM_003319.4:c.16991A=	NP_003310.4:p.His5664=
NM_133378.4:c.36482A=	NP_596869.4:p.His12161=
NM_133432.3:c.17366A=	NP_597676.3:p.His5789=
NM_133437.4:c.17567A=	NP_597681.4:p.His5856=
XM_011511729.1:c.43283A=	XP_011510031.1:p.His14428=
XM_011511730.1:c.17177A=	XP_011510032.1:p.His5726=
XM_011511731.1:c.17036A=	XP_011510033.1:p.His5679=
XM_017004819.1:c.43079A=	XP_016860308.1:p.His14360=
XM_017004820.1:c.38477A=	XP_016860309.1:p.His12826=
XM_017004821.1:c.38474A=	XP_016860310.1:p.His12825=
XM_017004822.1:c.35516A=	XP_016860311.1:p.His11839=
XM_017004823.1:c.17132A=	XP_016860312.1:p.His5711=
XM_024453094.1:c.38627A=	XP_024308862.1:p.His12876=
XM_024453095.1:c.38624A=	XP_024308863.1:p.His12875=
XM_024453096.1:c.38057A=	XP_024308864.1:p.His12686=
XM_024453097.1:c.35399A=	XP_024308865.1:p.His11800=
XM_024453098.1:c.35318A=	XP_024308866.1:p.His11773=
XM_024453099.1:c.17081A=	XP_024308867.1:p.His5694=
XM_024453100.1:c.6935A=	XP_024308868.1:p.His2312=