Canonical Allele Identifier: CA349569463

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178563028G>A , CM000664.2:g.178563028G>A	GRCh38
NC_000002.11:g.179427755G>A , CM000664.1:g.179427755G>A	GRCh37
NC_000002.10:g.179136001G>A	NCBI36
NG_011618.3:g.272775C>T , LRG_391:g.272775C>T
NG_051363.1:g.45202G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.83104C>T (TTN) MANE Select	NP_001254479.2:p.Arg27702Ter
ENST00000589042.5:c.83104C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg27702Ter
NM_001256850.1:c.78181C>T (TTN)	NP_001243779.1:p.Arg26061Ter
NM_003319.4:c.55909C>T (TTN)	NP_003310.4:p.Arg18637Ter
NM_133378.4:c.75400C>T (TTN)	NP_596869.4:p.Arg25134Ter
NM_133432.3:c.56284C>T (TTN)	NP_597676.3:p.Arg18762Ter
NM_133437.4:c.56485C>T (TTN)	NP_597681.4:p.Arg18829Ter
NR_038271.1:n.447-8272G>A (TTN-AS1)
NR_038272.1:n.2044-19544G>A (TTN-AS1)
ENST00000342175.10:c.56485C>T (TTN)	ENSP00000340554.6:p.Arg18829Ter
ENST00000342175.11:c.56485C>T (TTN)	ENSP00000340554.6:p.Arg18829Ter
ENST00000342992.10:c.75400C>T (TTN)	ENSP00000343764.6:p.Arg25134Ter
ENST00000342992.11:c.75400C>T (TTN)	ENSP00000343764.6:p.Arg25134Ter
ENST00000359218.10:c.56284C>T (TTN)	ENSP00000352154.5:p.Arg18762Ter
ENST00000359218.9:c.56284C>T (TTN)	ENSP00000352154.5:p.Arg18762Ter
ENST00000460472.6:c.55909C>T (TTN)	ENSP00000434586.1:p.Arg18637Ter
ENST00000591111.5:c.78181C>T (TTN)	ENSP00000465570.1:p.Arg26061Ter
ENST00000615779.4:c.78181C>T (TTN)	ENSP00000483597.1:p.Arg26061Ter
XM_011511729.1:c.82201C>T (TTN)	XP_011510031.1:p.Arg27401Ter
XM_011511730.1:c.56095C>T (TTN)	XP_011510032.1:p.Arg18699Ter
XM_011511731.1:c.55954C>T (TTN)	XP_011510033.1:p.Arg18652Ter
XM_017004819.1:c.81997C>T (TTN)	XP_016860308.1:p.Arg27333Ter
XM_017004820.1:c.77395C>T (TTN)	XP_016860309.1:p.Arg25799Ter
XM_017004821.1:c.77392C>T (TTN)	XP_016860310.1:p.Arg25798Ter
XM_017004822.1:c.74434C>T (TTN)	XP_016860311.1:p.Arg24812Ter
XM_017004823.1:c.56050C>T (TTN)	XP_016860312.1:p.Arg18684Ter
XM_024453094.1:c.77545C>T (TTN)	XP_024308862.1:p.Arg25849Ter
XM_024453095.1:c.77542C>T (TTN)	XP_024308863.1:p.Arg25848Ter
XM_024453096.1:c.76975C>T (TTN)	XP_024308864.1:p.Arg25659Ter
XM_024453097.1:c.74317C>T (TTN)	XP_024308865.1:p.Arg24773Ter
XM_024453098.1:c.74236C>T (TTN)	XP_024308866.1:p.Arg24746Ter
XM_024453099.1:c.55999C>T (TTN)	XP_024308867.1:p.Arg18667Ter
XM_024453100.1:c.45853C>T (TTN)	XP_024308868.1:p.Arg15285Ter