Canonical Allele Identifier: CA349592770

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178611462C>A , CM000664.2:g.178611462C>A	GRCh38
NC_000002.11:g.179476189C>A , CM000664.1:g.179476189C>A	GRCh37
NC_000002.10:g.179184434C>A	NCBI36
NG_011618.3:g.224341G>T , LRG_391:g.224341G>T
NG_051363.1:g.93636C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.50767G>T (TTN) MANE Select	NP_001254479.2:p.Glu16923Ter
ENST00000589042.5:c.50767G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu16923Ter
NM_001256850.1:c.45844G>T (TTN)	NP_001243779.1:p.Glu15282Ter
NM_003319.4:c.23572G>T (TTN)	NP_003310.4:p.Glu7858Ter
NM_133378.4:c.43063G>T (TTN)	NP_596869.4:p.Glu14355Ter
NM_133432.3:c.23947G>T (TTN)	NP_597676.3:p.Glu7983Ter
NM_133437.4:c.24148G>T (TTN)	NP_597681.4:p.Glu8050Ter
NR_038271.1:n.783-2573C>A (TTN-AS1)
ENST00000342175.10:c.24148G>T (TTN)	ENSP00000340554.6:p.Glu8050Ter
ENST00000342175.11:c.24148G>T (TTN)	ENSP00000340554.6:p.Glu8050Ter
ENST00000342992.10:c.43063G>T (TTN)	ENSP00000343764.6:p.Glu14355Ter
ENST00000342992.11:c.43063G>T (TTN)	ENSP00000343764.6:p.Glu14355Ter
ENST00000359218.10:c.23947G>T (TTN)	ENSP00000352154.5:p.Glu7983Ter
ENST00000359218.9:c.23947G>T (TTN)	ENSP00000352154.5:p.Glu7983Ter
ENST00000460472.6:c.23572G>T (TTN)	ENSP00000434586.1:p.Glu7858Ter
ENST00000591111.5:c.45844G>T (TTN)	ENSP00000465570.1:p.Glu15282Ter
ENST00000615779.4:c.45844G>T (TTN)	ENSP00000483597.1:p.Glu15282Ter
XM_011511729.1:c.49864G>T (TTN)	XP_011510031.1:p.Glu16622Ter
XM_011511730.1:c.23758G>T (TTN)	XP_011510032.1:p.Glu7920Ter
XM_011511731.1:c.23617G>T (TTN)	XP_011510033.1:p.Glu7873Ter
XM_017004819.1:c.49660G>T (TTN)	XP_016860308.1:p.Glu16554Ter
XM_017004820.1:c.45058G>T (TTN)	XP_016860309.1:p.Glu15020Ter
XM_017004821.1:c.45055G>T (TTN)	XP_016860310.1:p.Glu15019Ter
XM_017004822.1:c.42097G>T (TTN)	XP_016860311.1:p.Glu14033Ter
XM_017004823.1:c.23713G>T (TTN)	XP_016860312.1:p.Glu7905Ter
XM_024453094.1:c.45208G>T (TTN)	XP_024308862.1:p.Glu15070Ter
XM_024453095.1:c.45205G>T (TTN)	XP_024308863.1:p.Glu15069Ter
XM_024453096.1:c.44638G>T (TTN)	XP_024308864.1:p.Glu14880Ter
XM_024453097.1:c.41980G>T (TTN)	XP_024308865.1:p.Glu13994Ter
XM_024453098.1:c.41899G>T (TTN)	XP_024308866.1:p.Glu13967Ter
XM_024453099.1:c.23662G>T (TTN)	XP_024308867.1:p.Glu7888Ter
XM_024453100.1:c.13516G>T (TTN)	XP_024308868.1:p.Glu4506Ter