Canonical Allele Identifier: CA349441646

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586583T>A , CM000664.2:g.178586583T>A	GRCh38
NC_000002.11:g.179451310T>A , CM000664.1:g.179451310T>A	GRCh37
NC_000002.10:g.179159556T>A	NCBI36
NG_011618.3:g.249220A>T , LRG_391:g.249220A>T
NG_051363.1:g.68757T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.64318A>T (TTN) MANE Select	NP_001254479.2:p.Arg21440Ter
ENST00000589042.5:c.64318A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg21440Ter
NM_001256850.1:c.59395A>T (TTN)	NP_001243779.1:p.Arg19799Ter
NM_003319.4:c.37123A>T (TTN)	NP_003310.4:p.Arg12375Ter
NM_133378.4:c.56614A>T (TTN)	NP_596869.4:p.Arg18872Ter
NM_133432.3:c.37498A>T (TTN)	NP_597676.3:p.Arg12500Ter
NM_133437.4:c.37699A>T (TTN)	NP_597681.4:p.Arg12567Ter
NR_038271.1:n.597-11013T>A (TTN-AS1)
NR_038272.1:n.3188+1590T>A (TTN-AS1)
ENST00000342175.10:c.37699A>T (TTN)	ENSP00000340554.6:p.Arg12567Ter
ENST00000342175.11:c.37699A>T (TTN)	ENSP00000340554.6:p.Arg12567Ter
ENST00000342992.10:c.56614A>T (TTN)	ENSP00000343764.6:p.Arg18872Ter
ENST00000342992.11:c.56614A>T (TTN)	ENSP00000343764.6:p.Arg18872Ter
ENST00000359218.10:c.37498A>T (TTN)	ENSP00000352154.5:p.Arg12500Ter
ENST00000359218.9:c.37498A>T (TTN)	ENSP00000352154.5:p.Arg12500Ter
ENST00000460472.6:c.37123A>T (TTN)	ENSP00000434586.1:p.Arg12375Ter
ENST00000591111.5:c.59395A>T (TTN)	ENSP00000465570.1:p.Arg19799Ter
ENST00000615779.4:c.59395A>T (TTN)	ENSP00000483597.1:p.Arg19799Ter
XM_011511729.1:c.63415A>T (TTN)	XP_011510031.1:p.Arg21139Ter
XM_011511730.1:c.37309A>T (TTN)	XP_011510032.1:p.Arg12437Ter
XM_011511731.1:c.37168A>T (TTN)	XP_011510033.1:p.Arg12390Ter
XM_017004819.1:c.63211A>T (TTN)	XP_016860308.1:p.Arg21071Ter
XM_017004820.1:c.58609A>T (TTN)	XP_016860309.1:p.Arg19537Ter
XM_017004821.1:c.58606A>T (TTN)	XP_016860310.1:p.Arg19536Ter
XM_017004822.1:c.55648A>T (TTN)	XP_016860311.1:p.Arg18550Ter
XM_017004823.1:c.37264A>T (TTN)	XP_016860312.1:p.Arg12422Ter
XM_024453094.1:c.58759A>T (TTN)	XP_024308862.1:p.Arg19587Ter
XM_024453095.1:c.58756A>T (TTN)	XP_024308863.1:p.Arg19586Ter
XM_024453096.1:c.58189A>T (TTN)	XP_024308864.1:p.Arg19397Ter
XM_024453097.1:c.55531A>T (TTN)	XP_024308865.1:p.Arg18511Ter
XM_024453098.1:c.55450A>T (TTN)	XP_024308866.1:p.Arg18484Ter
XM_024453099.1:c.37213A>T (TTN)	XP_024308867.1:p.Arg12405Ter
XM_024453100.1:c.27067A>T (TTN)	XP_024308868.1:p.Arg9023Ter