Canonical Allele Identifier: CA1310532718

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178574497C= , CM000664.2:g.178574497C=	GRCh38
NC_000002.11:g.179439224C= , CM000664.1:g.179439224C=	GRCh37
NC_000002.10:g.179147470C=	NCBI36
NG_011618.3:g.261306G= , LRG_391:g.261306G=
NG_051363.1:g.56671C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.63931G= (TTN)	ENSP00000343764.6:p.Ala21311=
ENST00000342175.11:c.45016G= (TTN)	ENSP00000340554.6:p.Ala15006=
ENST00000359218.10:c.44815G= (TTN)	ENSP00000352154.5:p.Ala14939=
ENST00000342175.10:c.45016G= (TTN)	ENSP00000340554.6:p.Ala15006=
ENST00000342992.10:c.63931G= (TTN)	ENSP00000343764.6:p.Ala21311=
ENST00000359218.9:c.44815G= (TTN)	ENSP00000352154.5:p.Ala14939=
ENST00000460472.6:c.44440G= (TTN)	ENSP00000434586.1:p.Ala14814=
ENST00000589042.5:c.71635G= (TTN) MANE Select	ENSP00000467141.1:p.Ala23879=
ENST00000591111.5:c.66712G= (TTN)	ENSP00000465570.1:p.Ala22238=
ENST00000615779.4:c.66712G= (TTN)	ENSP00000483597.1:p.Ala22238=
NM_001256850.1:c.66712G= (TTN)	NP_001243779.1:p.Ala22238=
NM_001267550.2:c.71635G= (TTN) MANE Select	NP_001254479.2:p.Ala23879=
NM_003319.4:c.44440G= (TTN)	NP_003310.4:p.Ala14814=
NM_133378.4:c.63931G= (TTN)	NP_596869.4:p.Ala21311=
NM_133432.3:c.44815G= (TTN)	NP_597676.3:p.Ala14939=
NM_133437.4:c.45016G= (TTN)	NP_597681.4:p.Ala15006=
NR_038271.1:n.596+3048C= (TTN-AS1)
NR_038272.1:n.2044-8075C= (TTN-AS1)
XM_011511729.1:c.70732G= (TTN)	XP_011510031.1:p.Ala23578=
XM_011511730.1:c.44626G= (TTN)	XP_011510032.1:p.Ala14876=
XM_011511731.1:c.44485G= (TTN)	XP_011510033.1:p.Ala14829=
XM_017004819.1:c.70528G= (TTN)	XP_016860308.1:p.Ala23510=
XM_017004820.1:c.65926G= (TTN)	XP_016860309.1:p.Ala21976=
XM_017004821.1:c.65923G= (TTN)	XP_016860310.1:p.Ala21975=
XM_017004822.1:c.62965G= (TTN)	XP_016860311.1:p.Ala20989=
XM_017004823.1:c.44581G= (TTN)	XP_016860312.1:p.Ala14861=
XM_024453094.1:c.66076G= (TTN)	XP_024308862.1:p.Ala22026=
XM_024453095.1:c.66073G= (TTN)	XP_024308863.1:p.Ala22025=
XM_024453096.1:c.65506G= (TTN)	XP_024308864.1:p.Ala21836=
XM_024453097.1:c.62848G= (TTN)	XP_024308865.1:p.Ala20950=
XM_024453098.1:c.62767G= (TTN)	XP_024308866.1:p.Ala20923=
XM_024453099.1:c.44530G= (TTN)	XP_024308867.1:p.Ala14844=
XM_024453100.1:c.34384G= (TTN)	XP_024308868.1:p.Ala11462=