Canonical Allele Identifier: CA2662134708

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178618170-T-TTTAC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618174_178618177dup , CM000664.2:g.178618174_178618177dup	GRCh38
NC_000002.11:g.179482901_179482904dup , CM000664.1:g.179482901_179482904dup	GRCh37
NC_000002.10:g.179191146_179191149dup	NCBI36
NG_011618.3:g.217629_217632dup , LRG_391:g.217629_217632dup
NG_051363.1:g.100348_100351dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.39565+15_39565+18dup (TTN)	ENSP00000343764.6:n.39565+15_39565+18dup
ENST00000342175.11:c.20650+15_20650+18dup (TTN)	ENSP00000340554.6:n.20650+15_20650+18dup
ENST00000359218.10:c.20449+15_20449+18dup (TTN)	ENSP00000352154.5:n.20449+15_20449+18dup
ENST00000342175.10:c.20650+15_20650+18dup (TTN)	ENSP00000340554.6:n.20650+15_20650+18dup
ENST00000342992.10:c.39565+15_39565+18dup (TTN)	ENSP00000343764.6:n.39565+15_39565+18dup
ENST00000359218.9:c.20449+15_20449+18dup (TTN)	ENSP00000352154.5:n.20449+15_20449+18dup
ENST00000460472.6:c.20074+15_20074+18dup (TTN)	ENSP00000434586.1:n.20074+15_20074+18dup
ENST00000589042.5:c.47269+15_47269+18dup (TTN) MANE Select	ENSP00000467141.1:n.47269+15_47269+18dup
ENST00000591111.5:c.42346+15_42346+18dup (TTN)	ENSP00000465570.1:n.42346+15_42346+18dup
ENST00000615779.4:c.42346+15_42346+18dup (TTN)	ENSP00000483597.1:n.42346+15_42346+18dup
NM_001256850.1:c.42346+15_42346+18dup (TTN)	NP_001243779.1:n.42346+15_42346+18dup
NM_001267550.2:c.47269+15_47269+18dup (TTN) MANE Select	NP_001254479.2:n.47269+15_47269+18dup
NM_003319.4:c.20074+15_20074+18dup (TTN)	NP_003310.4:n.20074+15_20074+18dup
NM_133378.4:c.39565+15_39565+18dup (TTN)	NP_596869.4:n.39565+15_39565+18dup
NM_133432.3:c.20449+15_20449+18dup (TTN)	NP_597676.3:n.20449+15_20449+18dup
NM_133437.4:c.20650+15_20650+18dup (TTN)	NP_597681.4:n.20650+15_20650+18dup
NR_038271.1:n.1605-1579_1605-1576dup (TTN-AS1)
XM_011511729.1:c.46366+15_46366+18dup (TTN)	XP_011510031.1:n.46366+15_46366+18dup
XM_011511730.1:c.20260+15_20260+18dup (TTN)	XP_011510032.1:n.20260+15_20260+18dup
XM_011511731.1:c.20119+15_20119+18dup (TTN)	XP_011510033.1:n.20119+15_20119+18dup
XM_017004819.1:c.46162+15_46162+18dup (TTN)	XP_016860308.1:n.46162+15_46162+18dup
XM_017004820.1:c.41560+15_41560+18dup (TTN)	XP_016860309.1:n.41560+15_41560+18dup
XM_017004821.1:c.41557+15_41557+18dup (TTN)	XP_016860310.1:n.41557+15_41557+18dup
XM_017004822.1:c.38599+15_38599+18dup (TTN)	XP_016860311.1:n.38599+15_38599+18dup
XM_017004823.1:c.20215+15_20215+18dup (TTN)	XP_016860312.1:n.20215+15_20215+18dup
XM_024453094.1:c.41710+15_41710+18dup (TTN)	XP_024308862.1:n.41710+15_41710+18dup
XM_024453095.1:c.41707+15_41707+18dup (TTN)	XP_024308863.1:n.41707+15_41707+18dup
XM_024453096.1:c.41140+15_41140+18dup (TTN)	XP_024308864.1:n.41140+15_41140+18dup
XM_024453097.1:c.38482+15_38482+18dup (TTN)	XP_024308865.1:n.38482+15_38482+18dup
XM_024453098.1:c.38401+15_38401+18dup (TTN)	XP_024308866.1:n.38401+15_38401+18dup
XM_024453099.1:c.20164+15_20164+18dup (TTN)	XP_024308867.1:n.20164+15_20164+18dup
XM_024453100.1:c.10018+15_10018+18dup (TTN)	XP_024308868.1:n.10018+15_10018+18dup