Canonical Allele Identifier: CA2662147093

Gene: TTN

Linked Data

• gnomAD v4: 2-178689057-G-GGGA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689065_178689067dup , CM000664.2:g.178689065_178689067dup	GRCh38
NC_000002.11:g.179553792_179553794dup , CM000664.1:g.179553792_179553794dup	GRCh37
NC_000002.10:g.179262037_179262039dup	NCBI36
NG_011618.3:g.146743_146745dup , LRG_391:g.146743_146745dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.28356_28358dup	ENSP00000343764.6:p.Pro9453_Arg9454insPro
ENST00000342175.11:c.13859-46743_13859-46741dup	ENSP00000340554.6:n.13859-46743_13859-46741dup
ENST00000359218.10:c.13658-46743_13658-46741dup	ENSP00000352154.5:n.13658-46743_13658-46741dup
ENST00000342175.10:c.13859-46743_13859-46741dup	ENSP00000340554.6:n.13859-46743_13859-46741dup
ENST00000342992.10:c.28356_28358dup	ENSP00000343764.6:p.Pro9453_Arg9454insPro
ENST00000359218.9:c.13658-46743_13658-46741dup	ENSP00000352154.5:n.13658-46743_13658-46741dup
ENST00000414766.5:c.1722_1724dup	ENSP00000401501.1:p.Pro575_Arg576insPro
ENST00000460472.6:c.13283-46743_13283-46741dup	ENSP00000434586.1:n.13283-46743_13283-46741dup
ENST00000589042.5:c.32088_32090dup MANE Select	ENSP00000467141.1:p.Pro10697_Arg10698insPro
ENST00000591111.5:c.31137_31139dup	ENSP00000465570.1:p.Pro10380_Arg10381insPro
ENST00000615779.4:c.31137_31139dup	ENSP00000483597.1:p.Pro10380_Arg10381insPro
NM_001256850.1:c.31137_31139dup	NP_001243779.1:p.Pro10380_Arg10381insPro
NM_001267550.2:c.32088_32090dup MANE Select	NP_001254479.2:p.Pro10697_Arg10698insPro
NM_003319.4:c.13283-46743_13283-46741dup	NP_003310.4:n.13283-46743_13283-46741dup
NM_133378.4:c.28356_28358dup	NP_596869.4:p.Pro9453_Arg9454insPro
NM_133432.3:c.13658-46743_13658-46741dup	NP_597676.3:n.13658-46743_13658-46741dup
NM_133437.4:c.13859-46743_13859-46741dup	NP_597681.4:n.13859-46743_13859-46741dup
XM_011511729.1:c.31185_31187dup	XP_011510031.1:p.Pro10396_Arg10397insPro
XM_011511730.1:c.13469-46743_13469-46741dup	XP_011510032.1:n.13469-46743_13469-46741dup
XM_011511731.1:c.13328-46743_13328-46741dup	XP_011510033.1:n.13328-46743_13328-46741dup
XM_017004819.1:c.31140_31142dup	XP_016860308.1:p.Pro10381_Arg10382insPro
XM_017004820.1:c.28359_28361dup	XP_016860309.1:p.Pro9454_Arg9455insPro
XM_017004821.1:c.28356_28358dup	XP_016860310.1:p.Pro9453_Arg9454insPro
XM_017004822.1:c.31140_31142dup	XP_016860311.1:p.Pro10381_Arg10382insPro
XM_017004823.1:c.13424-46743_13424-46741dup	XP_016860312.1:n.13424-46743_13424-46741dup
XM_024453094.1:c.31140_31142dup	XP_024308862.1:p.Pro10381_Arg10382insPro
XM_024453095.1:c.31140_31142dup	XP_024308863.1:p.Pro10381_Arg10382insPro
XM_024453096.1:c.31140_31142dup	XP_024308864.1:p.Pro10381_Arg10382insPro
XM_024453097.1:c.30898+753_30898+755dup	XP_024308865.1:n.30898+753_30898+755dup
XM_024453098.1:c.30898+753_30898+755dup	XP_024308866.1:n.30898+753_30898+755dup
XM_024453099.1:c.13424-46743_13424-46741dup	XP_024308867.1:n.13424-46743_13424-46741dup