Canonical Allele Identifier: CA349460690

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178588983A>C , CM000664.2:g.178588983A>C	GRCh38
NC_000002.11:g.179453710A>C , CM000664.1:g.179453710A>C	GRCh37
NC_000002.10:g.179161956A>C	NCBI36
NG_011618.3:g.246820T>G , LRG_391:g.246820T>G
NG_051363.1:g.71157A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.62742T>G (TTN) MANE Select	NP_001254479.2:p.Tyr20914Ter
ENST00000589042.5:c.62742T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr20914Ter
NM_001256850.1:c.57819T>G (TTN)	NP_001243779.1:p.Tyr19273Ter
NM_003319.4:c.35547T>G (TTN)	NP_003310.4:p.Tyr11849Ter
NM_133378.4:c.55038T>G (TTN)	NP_596869.4:p.Tyr18346Ter
NM_133432.3:c.35922T>G (TTN)	NP_597676.3:p.Tyr11974Ter
NM_133437.4:c.36123T>G (TTN)	NP_597681.4:p.Tyr12041Ter
NR_038271.1:n.597-8613A>C (TTN-AS1)
NR_038272.1:n.3189-2156A>C (TTN-AS1)
ENST00000342175.10:c.36123T>G (TTN)	ENSP00000340554.6:p.Tyr12041Ter
ENST00000342175.11:c.36123T>G (TTN)	ENSP00000340554.6:p.Tyr12041Ter
ENST00000342992.10:c.55038T>G (TTN)	ENSP00000343764.6:p.Tyr18346Ter
ENST00000342992.11:c.55038T>G (TTN)	ENSP00000343764.6:p.Tyr18346Ter
ENST00000359218.10:c.35922T>G (TTN)	ENSP00000352154.5:p.Tyr11974Ter
ENST00000359218.9:c.35922T>G (TTN)	ENSP00000352154.5:p.Tyr11974Ter
ENST00000460472.6:c.35547T>G (TTN)	ENSP00000434586.1:p.Tyr11849Ter
ENST00000591111.5:c.57819T>G (TTN)	ENSP00000465570.1:p.Tyr19273Ter
ENST00000615779.4:c.57819T>G (TTN)	ENSP00000483597.1:p.Tyr19273Ter
XM_011511729.1:c.61839T>G (TTN)	XP_011510031.1:p.Tyr20613Ter
XM_011511730.1:c.35733T>G (TTN)	XP_011510032.1:p.Tyr11911Ter
XM_011511731.1:c.35592T>G (TTN)	XP_011510033.1:p.Tyr11864Ter
XM_017004819.1:c.61635T>G (TTN)	XP_016860308.1:p.Tyr20545Ter
XM_017004820.1:c.57033T>G (TTN)	XP_016860309.1:p.Tyr19011Ter
XM_017004821.1:c.57030T>G (TTN)	XP_016860310.1:p.Tyr19010Ter
XM_017004822.1:c.54072T>G (TTN)	XP_016860311.1:p.Tyr18024Ter
XM_017004823.1:c.35688T>G (TTN)	XP_016860312.1:p.Tyr11896Ter
XM_024453094.1:c.57183T>G (TTN)	XP_024308862.1:p.Tyr19061Ter
XM_024453095.1:c.57180T>G (TTN)	XP_024308863.1:p.Tyr19060Ter
XM_024453096.1:c.56613T>G (TTN)	XP_024308864.1:p.Tyr18871Ter
XM_024453097.1:c.53955T>G (TTN)	XP_024308865.1:p.Tyr17985Ter
XM_024453098.1:c.53874T>G (TTN)	XP_024308866.1:p.Tyr17958Ter
XM_024453099.1:c.35637T>G (TTN)	XP_024308867.1:p.Tyr11879Ter
XM_024453100.1:c.25491T>G (TTN)	XP_024308868.1:p.Tyr8497Ter