Canonical Allele Identifier: CA1310514680

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530488C= , CM000664.2:g.178530488C=	GRCh38
NC_000002.11:g.179395215C= , CM000664.1:g.179395215C=	GRCh37
NC_000002.10:g.179103461C=	NCBI36
NG_011618.3:g.305315G= , LRG_391:g.305315G=
NG_051363.1:g.12662C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98423G= (TTN)	ENSP00000343764.6:p.Gly32808=
ENST00000342175.11:c.79508G= (TTN)	ENSP00000340554.6:p.Gly26503=
ENST00000359218.10:c.79307G= (TTN)	ENSP00000352154.5:p.Gly26436=
ENST00000342175.10:c.79508G= (TTN)	ENSP00000340554.6:p.Gly26503=
ENST00000342992.10:c.98423G= (TTN)	ENSP00000343764.6:p.Gly32808=
ENST00000359218.9:c.79307G= (TTN)	ENSP00000352154.5:p.Gly26436=
ENST00000460472.6:c.78932G= (TTN)	ENSP00000434586.1:p.Gly26311=
ENST00000589042.5:c.106127G= (TTN) MANE Select	ENSP00000467141.1:p.Gly35376=
ENST00000591111.5:c.101204G= (TTN)	ENSP00000465570.1:p.Gly33735=
ENST00000615779.4:c.101204G= (TTN)	ENSP00000483597.1:p.Gly33735=
NM_001256850.1:c.101204G= (TTN)	NP_001243779.1:p.Gly33735=
NM_001267550.2:c.106127G= (TTN) MANE Select	NP_001254479.2:p.Gly35376=
NM_003319.4:c.78932G= (TTN)	NP_003310.4:p.Gly26311=
NM_133378.4:c.98423G= (TTN)	NP_596869.4:p.Gly32808=
NM_133432.3:c.79307G= (TTN)	NP_597676.3:p.Gly26436=
NM_133437.4:c.79508G= (TTN)	NP_597681.4:p.Gly26503=
NR_038271.1:n.446+6852C= (TTN-AS1)
NR_038272.1:n.220-5244C= (TTN-AS1)
XM_011511729.1:c.105224G= (TTN)	XP_011510031.1:p.Gly35075=
XM_011511730.1:c.79118G= (TTN)	XP_011510032.1:p.Gly26373=
XM_011511731.1:c.78977G= (TTN)	XP_011510033.1:p.Gly26326=
XM_017004819.1:c.105020G= (TTN)	XP_016860308.1:p.Gly35007=
XM_017004820.1:c.100418G= (TTN)	XP_016860309.1:p.Gly33473=
XM_017004821.1:c.100415G= (TTN)	XP_016860310.1:p.Gly33472=
XM_017004822.1:c.97457G= (TTN)	XP_016860311.1:p.Gly32486=
XM_017004823.1:c.79073G= (TTN)	XP_016860312.1:p.Gly26358=
XM_024453094.1:c.100568G= (TTN)	XP_024308862.1:p.Gly33523=
XM_024453095.1:c.100565G= (TTN)	XP_024308863.1:p.Gly33522=
XM_024453096.1:c.99998G= (TTN)	XP_024308864.1:p.Gly33333=
XM_024453097.1:c.97340G= (TTN)	XP_024308865.1:p.Gly32447=
XM_024453098.1:c.97259G= (TTN)	XP_024308866.1:p.Gly32420=
XM_024453099.1:c.79022G= (TTN)	XP_024308867.1:p.Gly26341=
XM_024453100.1:c.68876G= (TTN)	XP_024308868.1:p.Gly22959=