Canonical Allele Identifier: CA1310549127

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178613916C= , CM000664.2:g.178613916C=	GRCh38
NC_000002.11:g.179478643C= , CM000664.1:g.179478643C=	GRCh37
NC_000002.10:g.179186888C=	NCBI36
NG_011618.3:g.221887G= , LRG_391:g.221887G=
NG_051363.1:g.96090C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41663G= (TTN)	ENSP00000343764.6:p.Arg13888=
ENST00000342175.11:c.22748G= (TTN)	ENSP00000340554.6:p.Arg7583=
ENST00000359218.10:c.22547G= (TTN)	ENSP00000352154.5:p.Arg7516=
ENST00000342175.10:c.22748G= (TTN)	ENSP00000340554.6:p.Arg7583=
ENST00000342992.10:c.41663G= (TTN)	ENSP00000343764.6:p.Arg13888=
ENST00000359218.9:c.22547G= (TTN)	ENSP00000352154.5:p.Arg7516=
ENST00000460472.6:c.22172G= (TTN)	ENSP00000434586.1:p.Arg7391=
ENST00000589042.5:c.49367G= (TTN) MANE Select	ENSP00000467141.1:p.Arg16456=
ENST00000591111.5:c.44444G= (TTN)	ENSP00000465570.1:p.Arg14815=
ENST00000615779.4:c.44444G= (TTN)	ENSP00000483597.1:p.Arg14815=
NM_001256850.1:c.44444G= (TTN)	NP_001243779.1:p.Arg14815=
NM_001267550.2:c.49367G= (TTN) MANE Select	NP_001254479.2:p.Arg16456=
NM_003319.4:c.22172G= (TTN)	NP_003310.4:p.Arg7391=
NM_133378.4:c.41663G= (TTN)	NP_596869.4:p.Arg13888=
NM_133432.3:c.22547G= (TTN)	NP_597676.3:p.Arg7516=
NM_133437.4:c.22748G= (TTN)	NP_597681.4:p.Arg7583=
NR_038271.1:n.783-119C= (TTN-AS1)
XM_011511729.1:c.48464G= (TTN)	XP_011510031.1:p.Arg16155=
XM_011511730.1:c.22358G= (TTN)	XP_011510032.1:p.Arg7453=
XM_011511731.1:c.22217G= (TTN)	XP_011510033.1:p.Arg7406=
XM_017004819.1:c.48260G= (TTN)	XP_016860308.1:p.Arg16087=
XM_017004820.1:c.43658G= (TTN)	XP_016860309.1:p.Arg14553=
XM_017004821.1:c.43655G= (TTN)	XP_016860310.1:p.Arg14552=
XM_017004822.1:c.40697G= (TTN)	XP_016860311.1:p.Arg13566=
XM_017004823.1:c.22313G= (TTN)	XP_016860312.1:p.Arg7438=
XM_024453094.1:c.43808G= (TTN)	XP_024308862.1:p.Arg14603=
XM_024453095.1:c.43805G= (TTN)	XP_024308863.1:p.Arg14602=
XM_024453096.1:c.43238G= (TTN)	XP_024308864.1:p.Arg14413=
XM_024453097.1:c.40580G= (TTN)	XP_024308865.1:p.Arg13527=
XM_024453098.1:c.40499G= (TTN)	XP_024308866.1:p.Arg13500=
XM_024453099.1:c.22262G= (TTN)	XP_024308867.1:p.Arg7421=
XM_024453100.1:c.12116G= (TTN)	XP_024308868.1:p.Arg4039=