Canonical Allele Identifier: CA1310514628

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530431G= , CM000664.2:g.178530431G=	GRCh38
NC_000002.11:g.179395158G= , CM000664.1:g.179395158G=	GRCh37
NC_000002.10:g.179103404G=	NCBI36
NG_011618.3:g.305372C= , LRG_391:g.305372C=
NG_051363.1:g.12605G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98480C= (TTN)	ENSP00000343764.6:p.Ser32827=
ENST00000342175.11:c.79565C= (TTN)	ENSP00000340554.6:p.Ser26522=
ENST00000359218.10:c.79364C= (TTN)	ENSP00000352154.5:p.Ser26455=
ENST00000342175.10:c.79565C= (TTN)	ENSP00000340554.6:p.Ser26522=
ENST00000342992.10:c.98480C= (TTN)	ENSP00000343764.6:p.Ser32827=
ENST00000359218.9:c.79364C= (TTN)	ENSP00000352154.5:p.Ser26455=
ENST00000460472.6:c.78989C= (TTN)	ENSP00000434586.1:p.Ser26330=
ENST00000589042.5:c.106184C= (TTN) MANE Select	ENSP00000467141.1:p.Ser35395=
ENST00000591111.5:c.101261C= (TTN)	ENSP00000465570.1:p.Ser33754=
ENST00000615779.4:c.101261C= (TTN)	ENSP00000483597.1:p.Ser33754=
NM_001256850.1:c.101261C= (TTN)	NP_001243779.1:p.Ser33754=
NM_001267550.2:c.106184C= (TTN) MANE Select	NP_001254479.2:p.Ser35395=
NM_003319.4:c.78989C= (TTN)	NP_003310.4:p.Ser26330=
NM_133378.4:c.98480C= (TTN)	NP_596869.4:p.Ser32827=
NM_133432.3:c.79364C= (TTN)	NP_597676.3:p.Ser26455=
NM_133437.4:c.79565C= (TTN)	NP_597681.4:p.Ser26522=
NR_038271.1:n.446+6795G= (TTN-AS1)
NR_038272.1:n.220-5301G= (TTN-AS1)
XM_011511729.1:c.105281C= (TTN)	XP_011510031.1:p.Ser35094=
XM_011511730.1:c.79175C= (TTN)	XP_011510032.1:p.Ser26392=
XM_011511731.1:c.79034C= (TTN)	XP_011510033.1:p.Ser26345=
XM_017004819.1:c.105077C= (TTN)	XP_016860308.1:p.Ser35026=
XM_017004820.1:c.100475C= (TTN)	XP_016860309.1:p.Ser33492=
XM_017004821.1:c.100472C= (TTN)	XP_016860310.1:p.Ser33491=
XM_017004822.1:c.97514C= (TTN)	XP_016860311.1:p.Ser32505=
XM_017004823.1:c.79130C= (TTN)	XP_016860312.1:p.Ser26377=
XM_024453094.1:c.100625C= (TTN)	XP_024308862.1:p.Ser33542=
XM_024453095.1:c.100622C= (TTN)	XP_024308863.1:p.Ser33541=
XM_024453096.1:c.100055C= (TTN)	XP_024308864.1:p.Ser33352=
XM_024453097.1:c.97397C= (TTN)	XP_024308865.1:p.Ser32466=
XM_024453098.1:c.97316C= (TTN)	XP_024308866.1:p.Ser32439=
XM_024453099.1:c.79079C= (TTN)	XP_024308867.1:p.Ser26360=
XM_024453100.1:c.68933C= (TTN)	XP_024308868.1:p.Ser22978=