Canonical Allele Identifier: CA1310514703

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530512G= , CM000664.2:g.178530512G=	GRCh38
NC_000002.11:g.179395239G= , CM000664.1:g.179395239G=	GRCh37
NC_000002.10:g.179103485G=	NCBI36
NG_011618.3:g.305291C= , LRG_391:g.305291C=
NG_051363.1:g.12686G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98399C= (TTN)	ENSP00000343764.6:p.Ser32800=
ENST00000342175.11:c.79484C= (TTN)	ENSP00000340554.6:p.Ser26495=
ENST00000359218.10:c.79283C= (TTN)	ENSP00000352154.5:p.Ser26428=
ENST00000342175.10:c.79484C= (TTN)	ENSP00000340554.6:p.Ser26495=
ENST00000342992.10:c.98399C= (TTN)	ENSP00000343764.6:p.Ser32800=
ENST00000359218.9:c.79283C= (TTN)	ENSP00000352154.5:p.Ser26428=
ENST00000460472.6:c.78908C= (TTN)	ENSP00000434586.1:p.Ser26303=
ENST00000589042.5:c.106103C= (TTN) MANE Select	ENSP00000467141.1:p.Ser35368=
ENST00000591111.5:c.101180C= (TTN)	ENSP00000465570.1:p.Ser33727=
ENST00000615779.4:c.101180C= (TTN)	ENSP00000483597.1:p.Ser33727=
NM_001256850.1:c.101180C= (TTN)	NP_001243779.1:p.Ser33727=
NM_001267550.2:c.106103C= (TTN) MANE Select	NP_001254479.2:p.Ser35368=
NM_003319.4:c.78908C= (TTN)	NP_003310.4:p.Ser26303=
NM_133378.4:c.98399C= (TTN)	NP_596869.4:p.Ser32800=
NM_133432.3:c.79283C= (TTN)	NP_597676.3:p.Ser26428=
NM_133437.4:c.79484C= (TTN)	NP_597681.4:p.Ser26495=
NR_038271.1:n.446+6876G= (TTN-AS1)
NR_038272.1:n.220-5220G= (TTN-AS1)
XM_011511729.1:c.105200C= (TTN)	XP_011510031.1:p.Ser35067=
XM_011511730.1:c.79094C= (TTN)	XP_011510032.1:p.Ser26365=
XM_011511731.1:c.78953C= (TTN)	XP_011510033.1:p.Ser26318=
XM_017004819.1:c.104996C= (TTN)	XP_016860308.1:p.Ser34999=
XM_017004820.1:c.100394C= (TTN)	XP_016860309.1:p.Ser33465=
XM_017004821.1:c.100391C= (TTN)	XP_016860310.1:p.Ser33464=
XM_017004822.1:c.97433C= (TTN)	XP_016860311.1:p.Ser32478=
XM_017004823.1:c.79049C= (TTN)	XP_016860312.1:p.Ser26350=
XM_024453094.1:c.100544C= (TTN)	XP_024308862.1:p.Ser33515=
XM_024453095.1:c.100541C= (TTN)	XP_024308863.1:p.Ser33514=
XM_024453096.1:c.99974C= (TTN)	XP_024308864.1:p.Ser33325=
XM_024453097.1:c.97316C= (TTN)	XP_024308865.1:p.Ser32439=
XM_024453098.1:c.97235C= (TTN)	XP_024308866.1:p.Ser32412=
XM_024453099.1:c.78998C= (TTN)	XP_024308867.1:p.Ser26333=
XM_024453100.1:c.68852C= (TTN)	XP_024308868.1:p.Ser22951=