Canonical Allele Identifier: CA349442654

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178586685T>A , CM000664.2:g.178586685T>A	GRCh38
NC_000002.11:g.179451412T>A , CM000664.1:g.179451412T>A	GRCh37
NC_000002.10:g.179159658T>A	NCBI36
NG_011618.3:g.249118A>T , LRG_391:g.249118A>T
NG_051363.1:g.68859T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.64216A>T (TTN) MANE Select	NP_001254479.2:p.Arg21406Ter
ENST00000589042.5:c.64216A>T (TTN) MANE Select	ENSP00000467141.1:p.Arg21406Ter
NM_001256850.1:c.59293A>T (TTN)	NP_001243779.1:p.Arg19765Ter
NM_003319.4:c.37021A>T (TTN)	NP_003310.4:p.Arg12341Ter
NM_133378.4:c.56512A>T (TTN)	NP_596869.4:p.Arg18838Ter
NM_133432.3:c.37396A>T (TTN)	NP_597676.3:p.Arg12466Ter
NM_133437.4:c.37597A>T (TTN)	NP_597681.4:p.Arg12533Ter
NR_038271.1:n.597-10911T>A (TTN-AS1)
NR_038272.1:n.3188+1692T>A (TTN-AS1)
ENST00000342175.10:c.37597A>T (TTN)	ENSP00000340554.6:p.Arg12533Ter
ENST00000342175.11:c.37597A>T (TTN)	ENSP00000340554.6:p.Arg12533Ter
ENST00000342992.10:c.56512A>T (TTN)	ENSP00000343764.6:p.Arg18838Ter
ENST00000342992.11:c.56512A>T (TTN)	ENSP00000343764.6:p.Arg18838Ter
ENST00000359218.10:c.37396A>T (TTN)	ENSP00000352154.5:p.Arg12466Ter
ENST00000359218.9:c.37396A>T (TTN)	ENSP00000352154.5:p.Arg12466Ter
ENST00000460472.6:c.37021A>T (TTN)	ENSP00000434586.1:p.Arg12341Ter
ENST00000591111.5:c.59293A>T (TTN)	ENSP00000465570.1:p.Arg19765Ter
ENST00000615779.4:c.59293A>T (TTN)	ENSP00000483597.1:p.Arg19765Ter
XM_011511729.1:c.63313A>T (TTN)	XP_011510031.1:p.Arg21105Ter
XM_011511730.1:c.37207A>T (TTN)	XP_011510032.1:p.Arg12403Ter
XM_011511731.1:c.37066A>T (TTN)	XP_011510033.1:p.Arg12356Ter
XM_017004819.1:c.63109A>T (TTN)	XP_016860308.1:p.Arg21037Ter
XM_017004820.1:c.58507A>T (TTN)	XP_016860309.1:p.Arg19503Ter
XM_017004821.1:c.58504A>T (TTN)	XP_016860310.1:p.Arg19502Ter
XM_017004822.1:c.55546A>T (TTN)	XP_016860311.1:p.Arg18516Ter
XM_017004823.1:c.37162A>T (TTN)	XP_016860312.1:p.Arg12388Ter
XM_024453094.1:c.58657A>T (TTN)	XP_024308862.1:p.Arg19553Ter
XM_024453095.1:c.58654A>T (TTN)	XP_024308863.1:p.Arg19552Ter
XM_024453096.1:c.58087A>T (TTN)	XP_024308864.1:p.Arg19363Ter
XM_024453097.1:c.55429A>T (TTN)	XP_024308865.1:p.Arg18477Ter
XM_024453098.1:c.55348A>T (TTN)	XP_024308866.1:p.Arg18450Ter
XM_024453099.1:c.37111A>T (TTN)	XP_024308867.1:p.Arg12371Ter
XM_024453100.1:c.26965A>T (TTN)	XP_024308868.1:p.Arg8989Ter