Canonical Allele Identifier: CA1310518115

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532189_178532194delinsACTTCT , CM000664.2:g.178532189_178532194delinsACTTCT	GRCh38
NC_000002.11:g.179396916_179396921delinsACTTCT , CM000664.1:g.179396916_179396921delinsACTTCT	GRCh37
NC_000002.10:g.179105162_179105167delinsACTTCT	NCBI36
NG_011618.3:g.303609_303614delinsAGAAGT , LRG_391:g.303609_303614delinsAGAAGT
NG_051363.1:g.14363_14368delinsACTTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96717_96722delinsAGAAGT (TTN)	ENSP00000343764.6:p.Arg32239=
ENST00000342175.11:c.77802_77807delinsAGAAGT (TTN)	ENSP00000340554.6:p.Arg25934=
ENST00000359218.10:c.77601_77606delinsAGAAGT (TTN)	ENSP00000352154.5:p.Arg25867=
ENST00000342175.10:c.77802_77807delinsAGAAGT (TTN)	ENSP00000340554.6:p.Arg25934=
ENST00000342992.10:c.96717_96722delinsAGAAGT (TTN)	ENSP00000343764.6:p.Arg32239=
ENST00000359218.9:c.77601_77606delinsAGAAGT (TTN)	ENSP00000352154.5:p.Arg25867=
ENST00000460472.6:c.77226_77231delinsAGAAGT (TTN)	ENSP00000434586.1:p.Arg25742=
ENST00000589042.5:c.104421_104426delinsAGAAGT (TTN) MANE Select	ENSP00000467141.1:p.Arg34807=
ENST00000591111.5:c.99498_99503delinsAGAAGT (TTN)	ENSP00000465570.1:p.Arg33166=
ENST00000615779.4:c.99498_99503delinsAGAAGT (TTN)	ENSP00000483597.1:p.Arg33166=
NM_001256850.1:c.99498_99503delinsAGAAGT (TTN)	NP_001243779.1:p.Arg33166=
NM_001267550.2:c.104421_104426delinsAGAAGT (TTN) MANE Select	NP_001254479.2:p.Arg34807=
NM_003319.4:c.77226_77231delinsAGAAGT (TTN)	NP_003310.4:p.Arg25742=
NM_133378.4:c.96717_96722delinsAGAAGT (TTN)	NP_596869.4:p.Arg32239=
NM_133432.3:c.77601_77606delinsAGAAGT (TTN)	NP_597676.3:p.Arg25867=
NM_133437.4:c.77802_77807delinsAGAAGT (TTN)	NP_597681.4:p.Arg25934=
NR_038271.1:n.446+8553_446+8558delinsACTTCT (TTN-AS1)
NR_038272.1:n.220-3543_220-3538delinsACTTCT (TTN-AS1)
XM_011511729.1:c.103518_103523delinsAGAAGT (TTN)	XP_011510031.1:p.Arg34506=
XM_011511730.1:c.77412_77417delinsAGAAGT (TTN)	XP_011510032.1:p.Arg25804=
XM_011511731.1:c.77271_77276delinsAGAAGT (TTN)	XP_011510033.1:p.Arg25757=
XM_017004819.1:c.103314_103319delinsAGAAGT (TTN)	XP_016860308.1:p.Arg34438=
XM_017004820.1:c.98712_98717delinsAGAAGT (TTN)	XP_016860309.1:p.Arg32904=
XM_017004821.1:c.98709_98714delinsAGAAGT (TTN)	XP_016860310.1:p.Arg32903=
XM_017004822.1:c.95751_95756delinsAGAAGT (TTN)	XP_016860311.1:p.Arg31917=
XM_017004823.1:c.77367_77372delinsAGAAGT (TTN)	XP_016860312.1:p.Arg25789=
XM_024453094.1:c.98862_98867delinsAGAAGT (TTN)	XP_024308862.1:p.Arg32954=
XM_024453095.1:c.98859_98864delinsAGAAGT (TTN)	XP_024308863.1:p.Arg32953=
XM_024453096.1:c.98292_98297delinsAGAAGT (TTN)	XP_024308864.1:p.Arg32764=
XM_024453097.1:c.95634_95639delinsAGAAGT (TTN)	XP_024308865.1:p.Arg31878=
XM_024453098.1:c.95553_95558delinsAGAAGT (TTN)	XP_024308866.1:p.Arg31851=
XM_024453099.1:c.77316_77321delinsAGAAGT (TTN)	XP_024308867.1:p.Arg25772=
XM_024453100.1:c.67170_67175delinsAGAAGT (TTN)	XP_024308868.1:p.Arg22390=