Canonical Allele Identifier: CA1310523245

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546612G= , CM000664.2:g.178546612G=	GRCh38
NC_000002.11:g.179411339G= , CM000664.1:g.179411339G=	GRCh37
NC_000002.10:g.179119585G=	NCBI36
NG_011618.3:g.289191C= , LRG_391:g.289191C=
NG_051363.1:g.28786G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.94816C= (TTN) MANE Select	NP_001254479.2:p.Arg31606=
ENST00000589042.5:c.94816C= (TTN) MANE Select	ENSP00000467141.1:p.Arg31606=
NM_001256850.1:c.89893C= (TTN)	NP_001243779.1:p.Arg29965=
NM_003319.4:c.67621C= (TTN)	NP_003310.4:p.Arg22541=
NM_133378.4:c.87112C= (TTN)	NP_596869.4:p.Arg29038=
NM_133432.3:c.67996C= (TTN)	NP_597676.3:p.Arg22666=
NM_133437.4:c.68197C= (TTN)	NP_597681.4:p.Arg22733=
NR_038271.1:n.446+22976G= (TTN-AS1)
NR_038272.1:n.2043+4251G= (TTN-AS1)
ENST00000342175.10:c.68197C= (TTN)	ENSP00000340554.6:p.Arg22733=
ENST00000342175.11:c.68197C= (TTN)	ENSP00000340554.6:p.Arg22733=
ENST00000342992.10:c.87112C= (TTN)	ENSP00000343764.6:p.Arg29038=
ENST00000342992.11:c.87112C= (TTN)	ENSP00000343764.6:p.Arg29038=
ENST00000359218.10:c.67996C= (TTN)	ENSP00000352154.5:p.Arg22666=
ENST00000359218.9:c.67996C= (TTN)	ENSP00000352154.5:p.Arg22666=
ENST00000460472.6:c.67621C= (TTN)	ENSP00000434586.1:p.Arg22541=
ENST00000591111.5:c.89893C= (TTN)	ENSP00000465570.1:p.Arg29965=
ENST00000615779.4:c.89893C= (TTN)	ENSP00000483597.1:p.Arg29965=
XM_011511729.1:c.93913C= (TTN)	XP_011510031.1:p.Arg31305=
XM_011511730.1:c.67807C= (TTN)	XP_011510032.1:p.Arg22603=
XM_011511731.1:c.67666C= (TTN)	XP_011510033.1:p.Arg22556=
XM_017004819.1:c.93709C= (TTN)	XP_016860308.1:p.Arg31237=
XM_017004820.1:c.89107C= (TTN)	XP_016860309.1:p.Arg29703=
XM_017004821.1:c.89104C= (TTN)	XP_016860310.1:p.Arg29702=
XM_017004822.1:c.86146C= (TTN)	XP_016860311.1:p.Arg28716=
XM_017004823.1:c.67762C= (TTN)	XP_016860312.1:p.Arg22588=
XM_024453094.1:c.89257C= (TTN)	XP_024308862.1:p.Arg29753=
XM_024453095.1:c.89254C= (TTN)	XP_024308863.1:p.Arg29752=
XM_024453096.1:c.88687C= (TTN)	XP_024308864.1:p.Arg29563=
XM_024453097.1:c.86029C= (TTN)	XP_024308865.1:p.Arg28677=
XM_024453098.1:c.85948C= (TTN)	XP_024308866.1:p.Arg28650=
XM_024453099.1:c.67711C= (TTN)	XP_024308867.1:p.Arg22571=
XM_024453100.1:c.57565C= (TTN)	XP_024308868.1:p.Arg19189=