Canonical Allele Identifier: CA1310529892

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178567382_178567383delinsTA , CM000664.2:g.178567382_178567383delinsTA	GRCh38
NC_000002.11:g.179432109_179432110delinsTA , CM000664.1:g.179432109_179432110delinsTA	GRCh37
NC_000002.10:g.179140355_179140356delinsTA	NCBI36
NG_011618.3:g.268420_268421delinsTA , LRG_391:g.268420_268421delinsTA
NG_051363.1:g.49556_49557delinsTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.71045_71046delinsTA (TTN)	ENSP00000343764.6:p.Leu23682=
ENST00000342175.11:c.52130_52131delinsTA (TTN)	ENSP00000340554.6:p.Leu17377=
ENST00000359218.10:c.51929_51930delinsTA (TTN)	ENSP00000352154.5:p.Leu17310=
ENST00000342175.10:c.52130_52131delinsTA (TTN)	ENSP00000340554.6:p.Leu17377=
ENST00000342992.10:c.71045_71046delinsTA (TTN)	ENSP00000343764.6:p.Leu23682=
ENST00000359218.9:c.51929_51930delinsTA (TTN)	ENSP00000352154.5:p.Leu17310=
ENST00000460472.6:c.51554_51555delinsTA (TTN)	ENSP00000434586.1:p.Leu17185=
ENST00000589042.5:c.78749_78750delinsTA (TTN) MANE Select	ENSP00000467141.1:p.Leu26250=
ENST00000591111.5:c.73826_73827delinsTA (TTN)	ENSP00000465570.1:p.Leu24609=
ENST00000615779.4:c.73826_73827delinsTA (TTN)	ENSP00000483597.1:p.Leu24609=
NM_001256850.1:c.73826_73827delinsTA (TTN)	NP_001243779.1:p.Leu24609=
NM_001267550.2:c.78749_78750delinsTA (TTN) MANE Select	NP_001254479.2:p.Leu26250=
NM_003319.4:c.51554_51555delinsTA (TTN)	NP_003310.4:p.Leu17185=
NM_133378.4:c.71045_71046delinsTA (TTN)	NP_596869.4:p.Leu23682=
NM_133432.3:c.51929_51930delinsTA (TTN)	NP_597676.3:p.Leu17310=
NM_133437.4:c.52130_52131delinsTA (TTN)	NP_597681.4:p.Leu17377=
NR_038271.1:n.447-3918_447-3917delinsTA (TTN-AS1)
NR_038272.1:n.2044-15190_2044-15189delinsTA (TTN-AS1)
XM_011511729.1:c.77846_77847delinsTA (TTN)	XP_011510031.1:p.Leu25949=
XM_011511730.1:c.51740_51741delinsTA (TTN)	XP_011510032.1:p.Leu17247=
XM_011511731.1:c.51599_51600delinsTA (TTN)	XP_011510033.1:p.Leu17200=
XM_017004819.1:c.77642_77643delinsTA (TTN)	XP_016860308.1:p.Leu25881=
XM_017004820.1:c.73040_73041delinsTA (TTN)	XP_016860309.1:p.Leu24347=
XM_017004821.1:c.73037_73038delinsTA (TTN)	XP_016860310.1:p.Leu24346=
XM_017004822.1:c.70079_70080delinsTA (TTN)	XP_016860311.1:p.Leu23360=
XM_017004823.1:c.51695_51696delinsTA (TTN)	XP_016860312.1:p.Leu17232=
XM_024453094.1:c.73190_73191delinsTA (TTN)	XP_024308862.1:p.Leu24397=
XM_024453095.1:c.73187_73188delinsTA (TTN)	XP_024308863.1:p.Leu24396=
XM_024453096.1:c.72620_72621delinsTA (TTN)	XP_024308864.1:p.Leu24207=
XM_024453097.1:c.69962_69963delinsTA (TTN)	XP_024308865.1:p.Leu23321=
XM_024453098.1:c.69881_69882delinsTA (TTN)	XP_024308866.1:p.Leu23294=
XM_024453099.1:c.51644_51645delinsTA (TTN)	XP_024308867.1:p.Leu17215=
XM_024453100.1:c.41498_41499delinsTA (TTN)	XP_024308868.1:p.Leu13833=