Canonical Allele Identifier: CA349519330

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178553691C>A , CM000664.2:g.178553691C>A	GRCh38
NC_000002.11:g.179418418C>A , CM000664.1:g.179418418C>A	GRCh37
NC_000002.10:g.179126664C>A	NCBI36
NG_011618.3:g.282112G>T , LRG_391:g.282112G>T
NG_051363.1:g.35865C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.89314G>T (TTN) MANE Select	NP_001254479.2:p.Glu29772Ter
ENST00000589042.5:c.89314G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu29772Ter
NM_001256850.1:c.84391G>T (TTN)	NP_001243779.1:p.Glu28131Ter
NM_003319.4:c.62119G>T (TTN)	NP_003310.4:p.Glu20707Ter
NM_133378.4:c.81610G>T (TTN)	NP_596869.4:p.Glu27204Ter
NM_133432.3:c.62494G>T (TTN)	NP_597676.3:p.Glu20832Ter
NM_133437.4:c.62695G>T (TTN)	NP_597681.4:p.Glu20899Ter
NR_038271.1:n.447-17609C>A (TTN-AS1)
NR_038272.1:n.2043+11330C>A (TTN-AS1)
ENST00000342175.10:c.62695G>T (TTN)	ENSP00000340554.6:p.Glu20899Ter
ENST00000342175.11:c.62695G>T (TTN)	ENSP00000340554.6:p.Glu20899Ter
ENST00000342992.10:c.81610G>T (TTN)	ENSP00000343764.6:p.Glu27204Ter
ENST00000342992.11:c.81610G>T (TTN)	ENSP00000343764.6:p.Glu27204Ter
ENST00000359218.10:c.62494G>T (TTN)	ENSP00000352154.5:p.Glu20832Ter
ENST00000359218.9:c.62494G>T (TTN)	ENSP00000352154.5:p.Glu20832Ter
ENST00000460472.6:c.62119G>T (TTN)	ENSP00000434586.1:p.Glu20707Ter
ENST00000591111.5:c.84391G>T (TTN)	ENSP00000465570.1:p.Glu28131Ter
ENST00000615779.4:c.84391G>T (TTN)	ENSP00000483597.1:p.Glu28131Ter
XM_011511729.1:c.88411G>T (TTN)	XP_011510031.1:p.Glu29471Ter
XM_011511730.1:c.62305G>T (TTN)	XP_011510032.1:p.Glu20769Ter
XM_011511731.1:c.62164G>T (TTN)	XP_011510033.1:p.Glu20722Ter
XM_017004819.1:c.88207G>T (TTN)	XP_016860308.1:p.Glu29403Ter
XM_017004820.1:c.83605G>T (TTN)	XP_016860309.1:p.Glu27869Ter
XM_017004821.1:c.83602G>T (TTN)	XP_016860310.1:p.Glu27868Ter
XM_017004822.1:c.80644G>T (TTN)	XP_016860311.1:p.Glu26882Ter
XM_017004823.1:c.62260G>T (TTN)	XP_016860312.1:p.Glu20754Ter
XM_024453094.1:c.83755G>T (TTN)	XP_024308862.1:p.Glu27919Ter
XM_024453095.1:c.83752G>T (TTN)	XP_024308863.1:p.Glu27918Ter
XM_024453096.1:c.83185G>T (TTN)	XP_024308864.1:p.Glu27729Ter
XM_024453097.1:c.80527G>T (TTN)	XP_024308865.1:p.Glu26843Ter
XM_024453098.1:c.80446G>T (TTN)	XP_024308866.1:p.Glu26816Ter
XM_024453099.1:c.62209G>T (TTN)	XP_024308867.1:p.Glu20737Ter
XM_024453100.1:c.52063G>T (TTN)	XP_024308868.1:p.Glu17355Ter