Canonical Allele Identifier: CA1310520140

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178549852C= , CM000664.2:g.178549852C=	GRCh38
NC_000002.11:g.179414579C= , CM000664.1:g.179414579C=	GRCh37
NC_000002.10:g.179122825C=	NCBI36
NG_011618.3:g.285951G= , LRG_391:g.285951G=
NG_051363.1:g.32026C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.84166G= (TTN)	ENSP00000343764.6:p.Val28056=
ENST00000342175.11:c.65251G= (TTN)	ENSP00000340554.6:p.Val21751=
ENST00000359218.10:c.65050G= (TTN)	ENSP00000352154.5:p.Val21684=
ENST00000342175.10:c.65251G= (TTN)	ENSP00000340554.6:p.Val21751=
ENST00000342992.10:c.84166G= (TTN)	ENSP00000343764.6:p.Val28056=
ENST00000359218.9:c.65050G= (TTN)	ENSP00000352154.5:p.Val21684=
ENST00000460472.6:c.64675G= (TTN)	ENSP00000434586.1:p.Val21559=
ENST00000589042.5:c.91870G= (TTN) MANE Select	ENSP00000467141.1:p.Val30624=
ENST00000591111.5:c.86947G= (TTN)	ENSP00000465570.1:p.Val28983=
ENST00000615779.4:c.86947G= (TTN)	ENSP00000483597.1:p.Val28983=
NM_001256850.1:c.86947G= (TTN)	NP_001243779.1:p.Val28983=
NM_001267550.2:c.91870G= (TTN) MANE Select	NP_001254479.2:p.Val30624=
NM_003319.4:c.64675G= (TTN)	NP_003310.4:p.Val21559=
NM_133378.4:c.84166G= (TTN)	NP_596869.4:p.Val28056=
NM_133432.3:c.65050G= (TTN)	NP_597676.3:p.Val21684=
NM_133437.4:c.65251G= (TTN)	NP_597681.4:p.Val21751=
NR_038271.1:n.447-21448C= (TTN-AS1)
NR_038272.1:n.2043+7491C= (TTN-AS1)
XM_011511729.1:c.90967G= (TTN)	XP_011510031.1:p.Val30323=
XM_011511730.1:c.64861G= (TTN)	XP_011510032.1:p.Val21621=
XM_011511731.1:c.64720G= (TTN)	XP_011510033.1:p.Val21574=
XM_017004819.1:c.90763G= (TTN)	XP_016860308.1:p.Val30255=
XM_017004820.1:c.86161G= (TTN)	XP_016860309.1:p.Val28721=
XM_017004821.1:c.86158G= (TTN)	XP_016860310.1:p.Val28720=
XM_017004822.1:c.83200G= (TTN)	XP_016860311.1:p.Val27734=
XM_017004823.1:c.64816G= (TTN)	XP_016860312.1:p.Val21606=
XM_024453094.1:c.86311G= (TTN)	XP_024308862.1:p.Val28771=
XM_024453095.1:c.86308G= (TTN)	XP_024308863.1:p.Val28770=
XM_024453096.1:c.85741G= (TTN)	XP_024308864.1:p.Val28581=
XM_024453097.1:c.83083G= (TTN)	XP_024308865.1:p.Val27695=
XM_024453098.1:c.83002G= (TTN)	XP_024308866.1:p.Val27668=
XM_024453099.1:c.64765G= (TTN)	XP_024308867.1:p.Val21589=
XM_024453100.1:c.54619G= (TTN)	XP_024308868.1:p.Val18207=