Canonical Allele Identifier: CA1310530788

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178569886C= , CM000664.2:g.178569886C=	GRCh38
NC_000002.11:g.179434613C= , CM000664.1:g.179434613C=	GRCh37
NC_000002.10:g.179142859C=	NCBI36
NG_011618.3:g.265917G= , LRG_391:g.265917G=
NG_051363.1:g.52060C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.68542G= (TTN)	ENSP00000343764.6:p.Asp22848=
ENST00000342175.11:c.49627G= (TTN)	ENSP00000340554.6:p.Asp16543=
ENST00000359218.10:c.49426G= (TTN)	ENSP00000352154.5:p.Asp16476=
ENST00000342175.10:c.49627G= (TTN)	ENSP00000340554.6:p.Asp16543=
ENST00000342992.10:c.68542G= (TTN)	ENSP00000343764.6:p.Asp22848=
ENST00000359218.9:c.49426G= (TTN)	ENSP00000352154.5:p.Asp16476=
ENST00000460472.6:c.49051G= (TTN)	ENSP00000434586.1:p.Asp16351=
ENST00000589042.5:c.76246G= (TTN) MANE Select	ENSP00000467141.1:p.Asp25416=
ENST00000591111.5:c.71323G= (TTN)	ENSP00000465570.1:p.Asp23775=
ENST00000615779.4:c.71323G= (TTN)	ENSP00000483597.1:p.Asp23775=
NM_001256850.1:c.71323G= (TTN)	NP_001243779.1:p.Asp23775=
NM_001267550.2:c.76246G= (TTN) MANE Select	NP_001254479.2:p.Asp25416=
NM_003319.4:c.49051G= (TTN)	NP_003310.4:p.Asp16351=
NM_133378.4:c.68542G= (TTN)	NP_596869.4:p.Asp22848=
NM_133432.3:c.49426G= (TTN)	NP_597676.3:p.Asp16476=
NM_133437.4:c.49627G= (TTN)	NP_597681.4:p.Asp16543=
NR_038271.1:n.447-1414C= (TTN-AS1)
NR_038272.1:n.2044-12686C= (TTN-AS1)
XM_011511729.1:c.75343G= (TTN)	XP_011510031.1:p.Asp25115=
XM_011511730.1:c.49237G= (TTN)	XP_011510032.1:p.Asp16413=
XM_011511731.1:c.49096G= (TTN)	XP_011510033.1:p.Asp16366=
XM_017004819.1:c.75139G= (TTN)	XP_016860308.1:p.Asp25047=
XM_017004820.1:c.70537G= (TTN)	XP_016860309.1:p.Asp23513=
XM_017004821.1:c.70534G= (TTN)	XP_016860310.1:p.Asp23512=
XM_017004822.1:c.67576G= (TTN)	XP_016860311.1:p.Asp22526=
XM_017004823.1:c.49192G= (TTN)	XP_016860312.1:p.Asp16398=
XM_024453094.1:c.70687G= (TTN)	XP_024308862.1:p.Asp23563=
XM_024453095.1:c.70684G= (TTN)	XP_024308863.1:p.Asp23562=
XM_024453096.1:c.70117G= (TTN)	XP_024308864.1:p.Asp23373=
XM_024453097.1:c.67459G= (TTN)	XP_024308865.1:p.Asp22487=
XM_024453098.1:c.67378G= (TTN)	XP_024308866.1:p.Asp22460=
XM_024453099.1:c.49141G= (TTN)	XP_024308867.1:p.Asp16381=
XM_024453100.1:c.38995G= (TTN)	XP_024308868.1:p.Asp12999=