Canonical Allele Identifier: CA1310524221

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547742C= , CM000664.2:g.178547742C=	GRCh38
NC_000002.11:g.179412469C= , CM000664.1:g.179412469C=	GRCh37
NC_000002.10:g.179120715C=	NCBI36
NG_011618.3:g.288061G= , LRG_391:g.288061G=
NG_051363.1:g.29916C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86180G= (TTN)	ENSP00000343764.6:p.Gly28727=
ENST00000342175.11:c.67265G= (TTN)	ENSP00000340554.6:p.Gly22422=
ENST00000359218.10:c.67064G= (TTN)	ENSP00000352154.5:p.Gly22355=
ENST00000342175.10:c.67265G= (TTN)	ENSP00000340554.6:p.Gly22422=
ENST00000342992.10:c.86180G= (TTN)	ENSP00000343764.6:p.Gly28727=
ENST00000359218.9:c.67064G= (TTN)	ENSP00000352154.5:p.Gly22355=
ENST00000460472.6:c.66689G= (TTN)	ENSP00000434586.1:p.Gly22230=
ENST00000589042.5:c.93884G= (TTN) MANE Select	ENSP00000467141.1:p.Gly31295=
ENST00000591111.5:c.88961G= (TTN)	ENSP00000465570.1:p.Gly29654=
ENST00000615779.4:c.88961G= (TTN)	ENSP00000483597.1:p.Gly29654=
NM_001256850.1:c.88961G= (TTN)	NP_001243779.1:p.Gly29654=
NM_001267550.2:c.93884G= (TTN) MANE Select	NP_001254479.2:p.Gly31295=
NM_003319.4:c.66689G= (TTN)	NP_003310.4:p.Gly22230=
NM_133378.4:c.86180G= (TTN)	NP_596869.4:p.Gly28727=
NM_133432.3:c.67064G= (TTN)	NP_597676.3:p.Gly22355=
NM_133437.4:c.67265G= (TTN)	NP_597681.4:p.Gly22422=
NR_038271.1:n.447-23558C= (TTN-AS1)
NR_038272.1:n.2043+5381C= (TTN-AS1)
XM_011511729.1:c.92981G= (TTN)	XP_011510031.1:p.Gly30994=
XM_011511730.1:c.66875G= (TTN)	XP_011510032.1:p.Gly22292=
XM_011511731.1:c.66734G= (TTN)	XP_011510033.1:p.Gly22245=
XM_017004819.1:c.92777G= (TTN)	XP_016860308.1:p.Gly30926=
XM_017004820.1:c.88175G= (TTN)	XP_016860309.1:p.Gly29392=
XM_017004821.1:c.88172G= (TTN)	XP_016860310.1:p.Gly29391=
XM_017004822.1:c.85214G= (TTN)	XP_016860311.1:p.Gly28405=
XM_017004823.1:c.66830G= (TTN)	XP_016860312.1:p.Gly22277=
XM_024453094.1:c.88325G= (TTN)	XP_024308862.1:p.Gly29442=
XM_024453095.1:c.88322G= (TTN)	XP_024308863.1:p.Gly29441=
XM_024453096.1:c.87755G= (TTN)	XP_024308864.1:p.Gly29252=
XM_024453097.1:c.85097G= (TTN)	XP_024308865.1:p.Gly28366=
XM_024453098.1:c.85016G= (TTN)	XP_024308866.1:p.Gly28339=
XM_024453099.1:c.66779G= (TTN)	XP_024308867.1:p.Gly22260=
XM_024453100.1:c.56633G= (TTN)	XP_024308868.1:p.Gly18878=