Canonical Allele Identifier: CA349627765

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570901A>T , CM000664.2:g.178570901A>T	GRCh38
NC_000002.11:g.179435628A>T , CM000664.1:g.179435628A>T	GRCh37
NC_000002.10:g.179143874A>T	NCBI36
NG_011618.3:g.264902T>A , LRG_391:g.264902T>A
NG_051363.1:g.53075A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.75231T>A (TTN) MANE Select	NP_001254479.2:p.Tyr25077Ter
ENST00000589042.5:c.75231T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr25077Ter
NM_001256850.1:c.70308T>A (TTN)	NP_001243779.1:p.Tyr23436Ter
NM_003319.4:c.48036T>A (TTN)	NP_003310.4:p.Tyr16012Ter
NM_133378.4:c.67527T>A (TTN)	NP_596869.4:p.Tyr22509Ter
NM_133432.3:c.48411T>A (TTN)	NP_597676.3:p.Tyr16137Ter
NM_133437.4:c.48612T>A (TTN)	NP_597681.4:p.Tyr16204Ter
NR_038271.1:n.447-399A>T (TTN-AS1)
NR_038272.1:n.2044-11671A>T (TTN-AS1)
ENST00000342175.10:c.48612T>A (TTN)	ENSP00000340554.6:p.Tyr16204Ter
ENST00000342175.11:c.48612T>A (TTN)	ENSP00000340554.6:p.Tyr16204Ter
ENST00000342992.10:c.67527T>A (TTN)	ENSP00000343764.6:p.Tyr22509Ter
ENST00000342992.11:c.67527T>A (TTN)	ENSP00000343764.6:p.Tyr22509Ter
ENST00000359218.10:c.48411T>A (TTN)	ENSP00000352154.5:p.Tyr16137Ter
ENST00000359218.9:c.48411T>A (TTN)	ENSP00000352154.5:p.Tyr16137Ter
ENST00000460472.6:c.48036T>A (TTN)	ENSP00000434586.1:p.Tyr16012Ter
ENST00000591111.5:c.70308T>A (TTN)	ENSP00000465570.1:p.Tyr23436Ter
ENST00000615779.4:c.70308T>A (TTN)	ENSP00000483597.1:p.Tyr23436Ter
XM_011511729.1:c.74328T>A (TTN)	XP_011510031.1:p.Tyr24776Ter
XM_011511730.1:c.48222T>A (TTN)	XP_011510032.1:p.Tyr16074Ter
XM_011511731.1:c.48081T>A (TTN)	XP_011510033.1:p.Tyr16027Ter
XM_017004819.1:c.74124T>A (TTN)	XP_016860308.1:p.Tyr24708Ter
XM_017004820.1:c.69522T>A (TTN)	XP_016860309.1:p.Tyr23174Ter
XM_017004821.1:c.69519T>A (TTN)	XP_016860310.1:p.Tyr23173Ter
XM_017004822.1:c.66561T>A (TTN)	XP_016860311.1:p.Tyr22187Ter
XM_017004823.1:c.48177T>A (TTN)	XP_016860312.1:p.Tyr16059Ter
XM_024453094.1:c.69672T>A (TTN)	XP_024308862.1:p.Tyr23224Ter
XM_024453095.1:c.69669T>A (TTN)	XP_024308863.1:p.Tyr23223Ter
XM_024453096.1:c.69102T>A (TTN)	XP_024308864.1:p.Tyr23034Ter
XM_024453097.1:c.66444T>A (TTN)	XP_024308865.1:p.Tyr22148Ter
XM_024453098.1:c.66363T>A (TTN)	XP_024308866.1:p.Tyr22121Ter
XM_024453099.1:c.48126T>A (TTN)	XP_024308867.1:p.Tyr16042Ter
XM_024453100.1:c.37980T>A (TTN)	XP_024308868.1:p.Tyr12660Ter