Canonical Allele Identifier: CA1310518118

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532193C= , CM000664.2:g.178532193C=	GRCh38
NC_000002.11:g.179396920C= , CM000664.1:g.179396920C=	GRCh37
NC_000002.10:g.179105166C=	NCBI36
NG_011618.3:g.303610G= , LRG_391:g.303610G=
NG_051363.1:g.14367C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96718G= (TTN)	ENSP00000343764.6:p.Glu32240=
ENST00000342175.11:c.77803G= (TTN)	ENSP00000340554.6:p.Glu25935=
ENST00000359218.10:c.77602G= (TTN)	ENSP00000352154.5:p.Glu25868=
ENST00000342175.10:c.77803G= (TTN)	ENSP00000340554.6:p.Glu25935=
ENST00000342992.10:c.96718G= (TTN)	ENSP00000343764.6:p.Glu32240=
ENST00000359218.9:c.77602G= (TTN)	ENSP00000352154.5:p.Glu25868=
ENST00000460472.6:c.77227G= (TTN)	ENSP00000434586.1:p.Glu25743=
ENST00000589042.5:c.104422G= (TTN) MANE Select	ENSP00000467141.1:p.Glu34808=
ENST00000591111.5:c.99499G= (TTN)	ENSP00000465570.1:p.Glu33167=
ENST00000615779.4:c.99499G= (TTN)	ENSP00000483597.1:p.Glu33167=
NM_001256850.1:c.99499G= (TTN)	NP_001243779.1:p.Glu33167=
NM_001267550.2:c.104422G= (TTN) MANE Select	NP_001254479.2:p.Glu34808=
NM_003319.4:c.77227G= (TTN)	NP_003310.4:p.Glu25743=
NM_133378.4:c.96718G= (TTN)	NP_596869.4:p.Glu32240=
NM_133432.3:c.77602G= (TTN)	NP_597676.3:p.Glu25868=
NM_133437.4:c.77803G= (TTN)	NP_597681.4:p.Glu25935=
NR_038271.1:n.446+8557C= (TTN-AS1)
NR_038272.1:n.220-3539C= (TTN-AS1)
XM_011511729.1:c.103519G= (TTN)	XP_011510031.1:p.Glu34507=
XM_011511730.1:c.77413G= (TTN)	XP_011510032.1:p.Glu25805=
XM_011511731.1:c.77272G= (TTN)	XP_011510033.1:p.Glu25758=
XM_017004819.1:c.103315G= (TTN)	XP_016860308.1:p.Glu34439=
XM_017004820.1:c.98713G= (TTN)	XP_016860309.1:p.Glu32905=
XM_017004821.1:c.98710G= (TTN)	XP_016860310.1:p.Glu32904=
XM_017004822.1:c.95752G= (TTN)	XP_016860311.1:p.Glu31918=
XM_017004823.1:c.77368G= (TTN)	XP_016860312.1:p.Glu25790=
XM_024453094.1:c.98863G= (TTN)	XP_024308862.1:p.Glu32955=
XM_024453095.1:c.98860G= (TTN)	XP_024308863.1:p.Glu32954=
XM_024453096.1:c.98293G= (TTN)	XP_024308864.1:p.Glu32765=
XM_024453097.1:c.95635G= (TTN)	XP_024308865.1:p.Glu31879=
XM_024453098.1:c.95554G= (TTN)	XP_024308866.1:p.Glu31852=
XM_024453099.1:c.77317G= (TTN)	XP_024308867.1:p.Glu25773=
XM_024453100.1:c.67171G= (TTN)	XP_024308868.1:p.Glu22391=