Canonical Allele Identifier: CA349539214

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178558353T>A , CM000664.2:g.178558353T>A	GRCh38
NC_000002.11:g.179423080T>A , CM000664.1:g.179423080T>A	GRCh37
NC_000002.10:g.179131326T>A	NCBI36
NG_011618.3:g.277450A>T , LRG_391:g.277450A>T
NG_051363.1:g.40527T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.87106A>T (TTN) MANE Select	NP_001254479.2:p.Lys29036Ter
ENST00000589042.5:c.87106A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys29036Ter
NM_001256850.1:c.82183A>T (TTN)	NP_001243779.1:p.Lys27395Ter
NM_003319.4:c.59911A>T (TTN)	NP_003310.4:p.Lys19971Ter
NM_133378.4:c.79402A>T (TTN)	NP_596869.4:p.Lys26468Ter
NM_133432.3:c.60286A>T (TTN)	NP_597676.3:p.Lys20096Ter
NM_133437.4:c.60487A>T (TTN)	NP_597681.4:p.Lys20163Ter
NR_038271.1:n.447-12947T>A (TTN-AS1)
NR_038272.1:n.2043+15992T>A (TTN-AS1)
ENST00000342175.10:c.60487A>T (TTN)	ENSP00000340554.6:p.Lys20163Ter
ENST00000342175.11:c.60487A>T (TTN)	ENSP00000340554.6:p.Lys20163Ter
ENST00000342992.10:c.79402A>T (TTN)	ENSP00000343764.6:p.Lys26468Ter
ENST00000342992.11:c.79402A>T (TTN)	ENSP00000343764.6:p.Lys26468Ter
ENST00000359218.10:c.60286A>T (TTN)	ENSP00000352154.5:p.Lys20096Ter
ENST00000359218.9:c.60286A>T (TTN)	ENSP00000352154.5:p.Lys20096Ter
ENST00000460472.6:c.59911A>T (TTN)	ENSP00000434586.1:p.Lys19971Ter
ENST00000591111.5:c.82183A>T (TTN)	ENSP00000465570.1:p.Lys27395Ter
ENST00000615779.4:c.82183A>T (TTN)	ENSP00000483597.1:p.Lys27395Ter
XM_011511729.1:c.86203A>T (TTN)	XP_011510031.1:p.Lys28735Ter
XM_011511730.1:c.60097A>T (TTN)	XP_011510032.1:p.Lys20033Ter
XM_011511731.1:c.59956A>T (TTN)	XP_011510033.1:p.Lys19986Ter
XM_017004819.1:c.85999A>T (TTN)	XP_016860308.1:p.Lys28667Ter
XM_017004820.1:c.81397A>T (TTN)	XP_016860309.1:p.Lys27133Ter
XM_017004821.1:c.81394A>T (TTN)	XP_016860310.1:p.Lys27132Ter
XM_017004822.1:c.78436A>T (TTN)	XP_016860311.1:p.Lys26146Ter
XM_017004823.1:c.60052A>T (TTN)	XP_016860312.1:p.Lys20018Ter
XM_024453094.1:c.81547A>T (TTN)	XP_024308862.1:p.Lys27183Ter
XM_024453095.1:c.81544A>T (TTN)	XP_024308863.1:p.Lys27182Ter
XM_024453096.1:c.80977A>T (TTN)	XP_024308864.1:p.Lys26993Ter
XM_024453097.1:c.78319A>T (TTN)	XP_024308865.1:p.Lys26107Ter
XM_024453098.1:c.78238A>T (TTN)	XP_024308866.1:p.Lys26080Ter
XM_024453099.1:c.60001A>T (TTN)	XP_024308867.1:p.Lys20001Ter
XM_024453100.1:c.49855A>T (TTN)	XP_024308868.1:p.Lys16619Ter