Canonical Allele Identifier: CA2662123315

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178543708-C-CTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543713_178543717dup , CM000664.2:g.178543713_178543717dup	GRCh38
NC_000002.11:g.179408440_179408444dup , CM000664.1:g.179408440_179408444dup	GRCh37
NC_000002.10:g.179116686_179116690dup	NCBI36
NG_011618.3:g.292090_292094dup , LRG_391:g.292090_292094dup
NG_051363.1:g.25887_25891dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88607-51_88607-47dup (TTN)	ENSP00000343764.6:n.88607-51_88607-47dup
ENST00000342175.11:c.69692-51_69692-47dup (TTN)	ENSP00000340554.6:n.69692-51_69692-47dup
ENST00000359218.10:c.69491-51_69491-47dup (TTN)	ENSP00000352154.5:n.69491-51_69491-47dup
ENST00000342175.10:c.69692-51_69692-47dup (TTN)	ENSP00000340554.6:n.69692-51_69692-47dup
ENST00000342992.10:c.88607-51_88607-47dup (TTN)	ENSP00000343764.6:n.88607-51_88607-47dup
ENST00000359218.9:c.69491-51_69491-47dup (TTN)	ENSP00000352154.5:n.69491-51_69491-47dup
ENST00000460472.6:c.69116-51_69116-47dup (TTN)	ENSP00000434586.1:n.69116-51_69116-47dup
ENST00000589042.5:c.96311-51_96311-47dup (TTN) MANE Select	ENSP00000467141.1:n.96311-51_96311-47dup
ENST00000591111.5:c.91388-51_91388-47dup (TTN)	ENSP00000465570.1:n.91388-51_91388-47dup
ENST00000615779.4:c.91388-51_91388-47dup (TTN)	ENSP00000483597.1:n.91388-51_91388-47dup
NM_001256850.1:c.91388-51_91388-47dup (TTN)	NP_001243779.1:n.91388-51_91388-47dup
NM_001267550.2:c.96311-51_96311-47dup (TTN) MANE Select	NP_001254479.2:n.96311-51_96311-47dup
NM_003319.4:c.69116-51_69116-47dup (TTN)	NP_003310.4:n.69116-51_69116-47dup
NM_133378.4:c.88607-51_88607-47dup (TTN)	NP_596869.4:n.88607-51_88607-47dup
NM_133432.3:c.69491-51_69491-47dup (TTN)	NP_597676.3:n.69491-51_69491-47dup
NM_133437.4:c.69692-51_69692-47dup (TTN)	NP_597681.4:n.69692-51_69692-47dup
NR_038271.1:n.446+20077_446+20081dup (TTN-AS1)
NR_038272.1:n.2043+1352_2043+1356dup (TTN-AS1)
XM_011511729.1:c.95408-51_95408-47dup (TTN)	XP_011510031.1:n.95408-51_95408-47dup
XM_011511730.1:c.69302-51_69302-47dup (TTN)	XP_011510032.1:n.69302-51_69302-47dup
XM_011511731.1:c.69161-51_69161-47dup (TTN)	XP_011510033.1:n.69161-51_69161-47dup
XM_017004819.1:c.95204-51_95204-47dup (TTN)	XP_016860308.1:n.95204-51_95204-47dup
XM_017004820.1:c.90602-51_90602-47dup (TTN)	XP_016860309.1:n.90602-51_90602-47dup
XM_017004821.1:c.90599-51_90599-47dup (TTN)	XP_016860310.1:n.90599-51_90599-47dup
XM_017004822.1:c.87641-51_87641-47dup (TTN)	XP_016860311.1:n.87641-51_87641-47dup
XM_017004823.1:c.69257-51_69257-47dup (TTN)	XP_016860312.1:n.69257-51_69257-47dup
XM_024453094.1:c.90752-51_90752-47dup (TTN)	XP_024308862.1:n.90752-51_90752-47dup
XM_024453095.1:c.90749-51_90749-47dup (TTN)	XP_024308863.1:n.90749-51_90749-47dup
XM_024453096.1:c.90182-51_90182-47dup (TTN)	XP_024308864.1:n.90182-51_90182-47dup
XM_024453097.1:c.87524-51_87524-47dup (TTN)	XP_024308865.1:n.87524-51_87524-47dup
XM_024453098.1:c.87443-51_87443-47dup (TTN)	XP_024308866.1:n.87443-51_87443-47dup
XM_024453099.1:c.69206-51_69206-47dup (TTN)	XP_024308867.1:n.69206-51_69206-47dup
XM_024453100.1:c.59060-51_59060-47dup (TTN)	XP_024308868.1:n.59060-51_59060-47dup