Canonical Allele Identifier: CA1310519637

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178535790G= , CM000664.2:g.178535790G=	GRCh38
NC_000002.11:g.179400517G= , CM000664.1:g.179400517G=	GRCh37
NC_000002.10:g.179108763G=	NCBI36
NG_011618.3:g.300013C= , LRG_391:g.300013C=
NG_051363.1:g.17964G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.100825C= (TTN) MANE Select	NP_001254479.2:p.Arg33609=
ENST00000589042.5:c.100825C= (TTN) MANE Select	ENSP00000467141.1:p.Arg33609=
NM_001256850.1:c.95902C= (TTN)	NP_001243779.1:p.Arg31968=
NM_003319.4:c.73630C= (TTN)	NP_003310.4:p.Arg24544=
NM_133378.4:c.93121C= (TTN)	NP_596869.4:p.Arg31041=
NM_133432.3:c.74005C= (TTN)	NP_597676.3:p.Arg24669=
NM_133437.4:c.74206C= (TTN)	NP_597681.4:p.Arg24736=
NR_038271.1:n.446+12154G= (TTN-AS1)
NR_038272.1:n.278G= (TTN-AS1)
ENST00000342175.10:c.74206C= (TTN)	ENSP00000340554.6:p.Arg24736=
ENST00000342175.11:c.74206C= (TTN)	ENSP00000340554.6:p.Arg24736=
ENST00000342992.10:c.93121C= (TTN)	ENSP00000343764.6:p.Arg31041=
ENST00000342992.11:c.93121C= (TTN)	ENSP00000343764.6:p.Arg31041=
ENST00000359218.10:c.74005C= (TTN)	ENSP00000352154.5:p.Arg24669=
ENST00000359218.9:c.74005C= (TTN)	ENSP00000352154.5:p.Arg24669=
ENST00000460472.6:c.73630C= (TTN)	ENSP00000434586.1:p.Arg24544=
ENST00000591111.5:c.95902C= (TTN)	ENSP00000465570.1:p.Arg31968=
ENST00000615779.4:c.95902C= (TTN)	ENSP00000483597.1:p.Arg31968=
XM_011511729.1:c.99922C= (TTN)	XP_011510031.1:p.Arg33308=
XM_011511730.1:c.73816C= (TTN)	XP_011510032.1:p.Arg24606=
XM_011511731.1:c.73675C= (TTN)	XP_011510033.1:p.Arg24559=
XM_017004819.1:c.99718C= (TTN)	XP_016860308.1:p.Arg33240=
XM_017004820.1:c.95116C= (TTN)	XP_016860309.1:p.Arg31706=
XM_017004821.1:c.95113C= (TTN)	XP_016860310.1:p.Arg31705=
XM_017004822.1:c.92155C= (TTN)	XP_016860311.1:p.Arg30719=
XM_017004823.1:c.73771C= (TTN)	XP_016860312.1:p.Arg24591=
XM_024453094.1:c.95266C= (TTN)	XP_024308862.1:p.Arg31756=
XM_024453095.1:c.95263C= (TTN)	XP_024308863.1:p.Arg31755=
XM_024453096.1:c.94696C= (TTN)	XP_024308864.1:p.Arg31566=
XM_024453097.1:c.92038C= (TTN)	XP_024308865.1:p.Arg30680=
XM_024453098.1:c.91957C= (TTN)	XP_024308866.1:p.Arg30653=
XM_024453099.1:c.73720C= (TTN)	XP_024308867.1:p.Arg24574=
XM_024453100.1:c.63574C= (TTN)	XP_024308868.1:p.Arg21192=