Canonical Allele Identifier: CA1987724

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551990T>A , CM000664.2:g.178551990T>A	GRCh38
NC_000002.11:g.179416717T>A , CM000664.1:g.179416717T>A	GRCh37
NC_000002.10:g.179124963T>A	NCBI36
NG_011618.3:g.283813A>T , LRG_391:g.283813A>T
NG_051363.1:g.34164T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.90910A>T (TTN) MANE Select	NP_001254479.2:p.Arg30304Ter
ENST00000589042.5:c.90910A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg30304Ter
NM_001256850.1:c.85987A>T (TTN)	NP_001243779.1:p.Arg28663Ter
NM_003319.4:c.63715A>T (TTN)	NP_003310.4:p.Arg21239Ter
NM_133378.4:c.83206A>T (TTN)	NP_596869.4:p.Arg27736Ter
NM_133432.3:c.64090A>T (TTN)	NP_597676.3:p.Arg21364Ter
NM_133437.4:c.64291A>T (TTN)	NP_597681.4:p.Arg21431Ter
NR_038271.1:n.447-19310T>A (TTN-AS1)
NR_038272.1:n.2043+9629T>A (TTN-AS1)
ENST00000342175.10:c.64291A>T (TTN)	ENSP00000340554.6:p.Arg21431Ter
ENST00000342175.11:c.64291A>T (TTN)	ENSP00000340554.6:p.Arg21431Ter
ENST00000342992.10:c.83206A>T (TTN)	ENSP00000343764.6:p.Arg27736Ter
ENST00000342992.11:c.83206A>T (TTN)	ENSP00000343764.6:p.Arg27736Ter
ENST00000359218.10:c.64090A>T (TTN)	ENSP00000352154.5:p.Arg21364Ter
ENST00000359218.9:c.64090A>T (TTN)	ENSP00000352154.5:p.Arg21364Ter
ENST00000460472.6:c.63715A>T (TTN)	ENSP00000434586.1:p.Arg21239Ter
ENST00000591111.5:c.85987A>T (TTN)	ENSP00000465570.1:p.Arg28663Ter
ENST00000615779.4:c.85987A>T (TTN)	ENSP00000483597.1:p.Arg28663Ter
XM_011511729.1:c.90007A>T (TTN)	XP_011510031.1:p.Arg30003Ter
XM_011511730.1:c.63901A>T (TTN)	XP_011510032.1:p.Arg21301Ter
XM_011511731.1:c.63760A>T (TTN)	XP_011510033.1:p.Arg21254Ter
XM_017004819.1:c.89803A>T (TTN)	XP_016860308.1:p.Arg29935Ter
XM_017004820.1:c.85201A>T (TTN)	XP_016860309.1:p.Arg28401Ter
XM_017004821.1:c.85198A>T (TTN)	XP_016860310.1:p.Arg28400Ter
XM_017004822.1:c.82240A>T (TTN)	XP_016860311.1:p.Arg27414Ter
XM_017004823.1:c.63856A>T (TTN)	XP_016860312.1:p.Arg21286Ter
XM_024453094.1:c.85351A>T (TTN)	XP_024308862.1:p.Arg28451Ter
XM_024453095.1:c.85348A>T (TTN)	XP_024308863.1:p.Arg28450Ter
XM_024453096.1:c.84781A>T (TTN)	XP_024308864.1:p.Arg28261Ter
XM_024453097.1:c.82123A>T (TTN)	XP_024308865.1:p.Arg27375Ter
XM_024453098.1:c.82042A>T (TTN)	XP_024308866.1:p.Arg27348Ter
XM_024453099.1:c.63805A>T (TTN)	XP_024308867.1:p.Arg21269Ter
XM_024453100.1:c.53659A>T (TTN)	XP_024308868.1:p.Arg17887Ter