Canonical Allele Identifier: CA1310518096

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532139G= , CM000664.2:g.178532139G=	GRCh38
NC_000002.11:g.179396866G= , CM000664.1:g.179396866G=	GRCh37
NC_000002.10:g.179105112G=	NCBI36
NG_011618.3:g.303664C= , LRG_391:g.303664C=
NG_051363.1:g.14313G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96772C= (TTN)	ENSP00000343764.6:p.Gln32258=
ENST00000342175.11:c.77857C= (TTN)	ENSP00000340554.6:p.Gln25953=
ENST00000359218.10:c.77656C= (TTN)	ENSP00000352154.5:p.Gln25886=
ENST00000342175.10:c.77857C= (TTN)	ENSP00000340554.6:p.Gln25953=
ENST00000342992.10:c.96772C= (TTN)	ENSP00000343764.6:p.Gln32258=
ENST00000359218.9:c.77656C= (TTN)	ENSP00000352154.5:p.Gln25886=
ENST00000460472.6:c.77281C= (TTN)	ENSP00000434586.1:p.Gln25761=
ENST00000589042.5:c.104476C= (TTN) MANE Select	ENSP00000467141.1:p.Gln34826=
ENST00000591111.5:c.99553C= (TTN)	ENSP00000465570.1:p.Gln33185=
ENST00000615779.4:c.99553C= (TTN)	ENSP00000483597.1:p.Gln33185=
NM_001256850.1:c.99553C= (TTN)	NP_001243779.1:p.Gln33185=
NM_001267550.2:c.104476C= (TTN) MANE Select	NP_001254479.2:p.Gln34826=
NM_003319.4:c.77281C= (TTN)	NP_003310.4:p.Gln25761=
NM_133378.4:c.96772C= (TTN)	NP_596869.4:p.Gln32258=
NM_133432.3:c.77656C= (TTN)	NP_597676.3:p.Gln25886=
NM_133437.4:c.77857C= (TTN)	NP_597681.4:p.Gln25953=
NR_038271.1:n.446+8503G= (TTN-AS1)
NR_038272.1:n.220-3593G= (TTN-AS1)
XM_011511729.1:c.103573C= (TTN)	XP_011510031.1:p.Gln34525=
XM_011511730.1:c.77467C= (TTN)	XP_011510032.1:p.Gln25823=
XM_011511731.1:c.77326C= (TTN)	XP_011510033.1:p.Gln25776=
XM_017004819.1:c.103369C= (TTN)	XP_016860308.1:p.Gln34457=
XM_017004820.1:c.98767C= (TTN)	XP_016860309.1:p.Gln32923=
XM_017004821.1:c.98764C= (TTN)	XP_016860310.1:p.Gln32922=
XM_017004822.1:c.95806C= (TTN)	XP_016860311.1:p.Gln31936=
XM_017004823.1:c.77422C= (TTN)	XP_016860312.1:p.Gln25808=
XM_024453094.1:c.98917C= (TTN)	XP_024308862.1:p.Gln32973=
XM_024453095.1:c.98914C= (TTN)	XP_024308863.1:p.Gln32972=
XM_024453096.1:c.98347C= (TTN)	XP_024308864.1:p.Gln32783=
XM_024453097.1:c.95689C= (TTN)	XP_024308865.1:p.Gln31897=
XM_024453098.1:c.95608C= (TTN)	XP_024308866.1:p.Gln31870=
XM_024453099.1:c.77371C= (TTN)	XP_024308867.1:p.Gln25791=
XM_024453100.1:c.67225C= (TTN)	XP_024308868.1:p.Gln22409=