Canonical Allele Identifier: CA1310518120

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532195_178532197delinsCTT , CM000664.2:g.178532195_178532197delinsCTT	GRCh38
NC_000002.11:g.179396922_179396924delinsCTT , CM000664.1:g.179396922_179396924delinsCTT	GRCh37
NC_000002.10:g.179105168_179105170delinsCTT	NCBI36
NG_011618.3:g.303606_303608delinsAAG , LRG_391:g.303606_303608delinsAAG
NG_051363.1:g.14369_14371delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96714_96716delinsAAG (TTN)	ENSP00000343764.6:p.Gln32238=
ENST00000342175.11:c.77799_77801delinsAAG (TTN)	ENSP00000340554.6:p.Gln25933=
ENST00000359218.10:c.77598_77600delinsAAG (TTN)	ENSP00000352154.5:p.Gln25866=
ENST00000342175.10:c.77799_77801delinsAAG (TTN)	ENSP00000340554.6:p.Gln25933=
ENST00000342992.10:c.96714_96716delinsAAG (TTN)	ENSP00000343764.6:p.Gln32238=
ENST00000359218.9:c.77598_77600delinsAAG (TTN)	ENSP00000352154.5:p.Gln25866=
ENST00000460472.6:c.77223_77225delinsAAG (TTN)	ENSP00000434586.1:p.Gln25741=
ENST00000589042.5:c.104418_104420delinsAAG (TTN) MANE Select	ENSP00000467141.1:p.Gln34806=
ENST00000591111.5:c.99495_99497delinsAAG (TTN)	ENSP00000465570.1:p.Gln33165=
ENST00000615779.4:c.99495_99497delinsAAG (TTN)	ENSP00000483597.1:p.Gln33165=
NM_001256850.1:c.99495_99497delinsAAG (TTN)	NP_001243779.1:p.Gln33165=
NM_001267550.2:c.104418_104420delinsAAG (TTN) MANE Select	NP_001254479.2:p.Gln34806=
NM_003319.4:c.77223_77225delinsAAG (TTN)	NP_003310.4:p.Gln25741=
NM_133378.4:c.96714_96716delinsAAG (TTN)	NP_596869.4:p.Gln32238=
NM_133432.3:c.77598_77600delinsAAG (TTN)	NP_597676.3:p.Gln25866=
NM_133437.4:c.77799_77801delinsAAG (TTN)	NP_597681.4:p.Gln25933=
NR_038271.1:n.446+8559_446+8561delinsCTT (TTN-AS1)
NR_038272.1:n.220-3537_220-3535delinsCTT (TTN-AS1)
XM_011511729.1:c.103515_103517delinsAAG (TTN)	XP_011510031.1:p.Gln34505=
XM_011511730.1:c.77409_77411delinsAAG (TTN)	XP_011510032.1:p.Gln25803=
XM_011511731.1:c.77268_77270delinsAAG (TTN)	XP_011510033.1:p.Gln25756=
XM_017004819.1:c.103311_103313delinsAAG (TTN)	XP_016860308.1:p.Gln34437=
XM_017004820.1:c.98709_98711delinsAAG (TTN)	XP_016860309.1:p.Gln32903=
XM_017004821.1:c.98706_98708delinsAAG (TTN)	XP_016860310.1:p.Gln32902=
XM_017004822.1:c.95748_95750delinsAAG (TTN)	XP_016860311.1:p.Gln31916=
XM_017004823.1:c.77364_77366delinsAAG (TTN)	XP_016860312.1:p.Gln25788=
XM_024453094.1:c.98859_98861delinsAAG (TTN)	XP_024308862.1:p.Gln32953=
XM_024453095.1:c.98856_98858delinsAAG (TTN)	XP_024308863.1:p.Gln32952=
XM_024453096.1:c.98289_98291delinsAAG (TTN)	XP_024308864.1:p.Gln32763=
XM_024453097.1:c.95631_95633delinsAAG (TTN)	XP_024308865.1:p.Gln31877=
XM_024453098.1:c.95550_95552delinsAAG (TTN)	XP_024308866.1:p.Gln31850=
XM_024453099.1:c.77313_77315delinsAAG (TTN)	XP_024308867.1:p.Gln25771=
XM_024453100.1:c.67167_67169delinsAAG (TTN)	XP_024308868.1:p.Gln22389=