Canonical Allele Identifier: CA2536411824

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543899_178543901dup , CM000664.2:g.178543899_178543901dup	GRCh38
NC_000002.11:g.179408626_179408628dup , CM000664.1:g.179408626_179408628dup	GRCh37
NC_000002.10:g.179116872_179116874dup	NCBI36
NG_011618.3:g.291903_291905dup , LRG_391:g.291903_291905dup
NG_051363.1:g.26073_26075dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88540_88542dup (TTN)	ENSP00000343764.6:p.Lys29514_Tyr29515insLys
ENST00000342175.11:c.69625_69627dup (TTN)	ENSP00000340554.6:p.Lys23209_Tyr23210insLys
ENST00000359218.10:c.69424_69426dup (TTN)	ENSP00000352154.5:p.Lys23142_Tyr23143insLys
ENST00000342175.10:c.69625_69627dup (TTN)	ENSP00000340554.6:p.Lys23209_Tyr23210insLys
ENST00000342992.10:c.88540_88542dup (TTN)	ENSP00000343764.6:p.Lys29514_Tyr29515insLys
ENST00000359218.9:c.69424_69426dup (TTN)	ENSP00000352154.5:p.Lys23142_Tyr23143insLys
ENST00000460472.6:c.69049_69051dup (TTN)	ENSP00000434586.1:p.Lys23017_Tyr23018insLys
ENST00000589042.5:c.96244_96246dup (TTN) MANE Select	ENSP00000467141.1:p.Lys32082_Tyr32083insLys
ENST00000591111.5:c.91321_91323dup (TTN)	ENSP00000465570.1:p.Lys30441_Tyr30442insLys
ENST00000615779.4:c.91321_91323dup (TTN)	ENSP00000483597.1:p.Lys30441_Tyr30442insLys
NM_001256850.1:c.91321_91323dup (TTN)	NP_001243779.1:p.Lys30441_Tyr30442insLys
NM_001267550.2:c.96244_96246dup (TTN) MANE Select	NP_001254479.2:p.Lys32082_Tyr32083insLys
NM_003319.4:c.69049_69051dup (TTN)	NP_003310.4:p.Lys23017_Tyr23018insLys
NM_133378.4:c.88540_88542dup (TTN)	NP_596869.4:p.Lys29514_Tyr29515insLys
NM_133432.3:c.69424_69426dup (TTN)	NP_597676.3:p.Lys23142_Tyr23143insLys
NM_133437.4:c.69625_69627dup (TTN)	NP_597681.4:p.Lys23209_Tyr23210insLys
NR_038271.1:n.446+20263_446+20265dup (TTN-AS1)
NR_038272.1:n.2043+1538_2043+1540dup (TTN-AS1)
XM_011511729.1:c.95341_95343dup (TTN)	XP_011510031.1:p.Lys31781_Tyr31782insLys
XM_011511730.1:c.69235_69237dup (TTN)	XP_011510032.1:p.Lys23079_Tyr23080insLys
XM_011511731.1:c.69094_69096dup (TTN)	XP_011510033.1:p.Lys23032_Tyr23033insLys
XM_017004819.1:c.95137_95139dup (TTN)	XP_016860308.1:p.Lys31713_Tyr31714insLys
XM_017004820.1:c.90535_90537dup (TTN)	XP_016860309.1:p.Lys30179_Tyr30180insLys
XM_017004821.1:c.90532_90534dup (TTN)	XP_016860310.1:p.Lys30178_Tyr30179insLys
XM_017004822.1:c.87574_87576dup (TTN)	XP_016860311.1:p.Lys29192_Tyr29193insLys
XM_017004823.1:c.69190_69192dup (TTN)	XP_016860312.1:p.Lys23064_Tyr23065insLys
XM_024453094.1:c.90685_90687dup (TTN)	XP_024308862.1:p.Lys30229_Tyr30230insLys
XM_024453095.1:c.90682_90684dup (TTN)	XP_024308863.1:p.Lys30228_Tyr30229insLys
XM_024453096.1:c.90115_90117dup (TTN)	XP_024308864.1:p.Lys30039_Tyr30040insLys
XM_024453097.1:c.87457_87459dup (TTN)	XP_024308865.1:p.Lys29153_Tyr29154insLys
XM_024453098.1:c.87376_87378dup (TTN)	XP_024308866.1:p.Lys29126_Tyr29127insLys
XM_024453099.1:c.69139_69141dup (TTN)	XP_024308867.1:p.Lys23047_Tyr23048insLys
XM_024453100.1:c.58993_58995dup (TTN)	XP_024308868.1:p.Lys19665_Tyr19666insLys