Canonical Allele Identifier: CA538093355

Gene: TTN

Linked Data

• dbSNP Id: rs1577044020
• gnomAD v2: 2-179523384-CAGT-C
• MyVariant Identifiers: chr2:g.179523385_179523387del (hg19) ; chr2:g.178658658_178658660del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178658658_178658660del , CM000664.2:g.178658658_178658660del	GRCh38
NC_000002.11:g.179523385_179523387del , CM000664.1:g.179523385_179523387del	GRCh37
NC_000002.10:g.179231630_179231632del	NCBI36
NG_011618.3:g.177143_177145del , LRG_391:g.177143_177145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.31741+345_31741+347del	ENSP00000343764.6:n.31741+345_31741+347del
ENST00000342175.11:c.13859-16343_13859-16341del	ENSP00000340554.6:n.13859-16343_13859-16341del
ENST00000359218.10:c.13658-16343_13658-16341del	ENSP00000352154.5:n.13658-16343_13658-16341del
ENST00000342175.10:c.13859-16343_13859-16341del	ENSP00000340554.6:n.13859-16343_13859-16341del
ENST00000342992.10:c.31741+345_31741+347del	ENSP00000343764.6:n.31741+345_31741+347del
ENST00000359218.9:c.13658-16343_13658-16341del	ENSP00000352154.5:n.13658-16343_13658-16341del
ENST00000414766.5:c.2440+14973_2440+14975del	ENSP00000401501.1:n.2440+14973_2440+14975del
ENST00000460472.6:c.13283-16343_13283-16341del	ENSP00000434586.1:n.13283-16343_13283-16341del
ENST00000589042.5:c.37543+45_37543+47del MANE Select	ENSP00000467141.1:n.37543+45_37543+47del
ENST00000591111.5:c.34354+45_34354+47del	ENSP00000465570.1:n.34354+45_34354+47del
ENST00000615779.4:c.34522+345_34522+347del	ENSP00000483597.1:n.34522+345_34522+347del
NM_001256850.1:c.34522+345_34522+347del	NP_001243779.1:n.34522+345_34522+347del
NM_001267550.2:c.37543+45_37543+47del MANE Select	NP_001254479.2:n.37543+45_37543+47del
NM_003319.4:c.13283-16343_13283-16341del	NP_003310.4:n.13283-16343_13283-16341del
NM_133378.4:c.31741+345_31741+347del	NP_596869.4:n.31741+345_31741+347del
NM_133432.3:c.13658-16343_13658-16341del	NP_597676.3:n.13658-16343_13658-16341del
NM_133437.4:c.13859-16343_13859-16341del	NP_597681.4:n.13859-16343_13859-16341del
XM_011511729.1:c.36640+45_36640+47del	XP_011510031.1:n.36640+45_36640+47del
XM_011511730.1:c.13469-16343_13469-16341del	XP_011510032.1:n.13469-16343_13469-16341del
XM_011511731.1:c.13328-16343_13328-16341del	XP_011510033.1:n.13328-16343_13328-16341del
XM_017004819.1:c.36436+45_36436+47del	XP_016860308.1:n.36436+45_36436+47del
XM_017004820.1:c.31834+45_31834+47del	XP_016860309.1:n.31834+45_31834+47del
XM_017004821.1:c.31831+45_31831+47del	XP_016860310.1:n.31831+45_31831+47del
XM_017004822.1:c.31858+14973_31858+14975del	XP_016860311.1:n.31858+14973_31858+14975del
XM_017004823.1:c.13424-16343_13424-16341del	XP_016860312.1:n.13424-16343_13424-16341del
XM_024453094.1:c.33478+45_33478+47del	XP_024308862.1:n.33478+45_33478+47del
XM_024453095.1:c.33475+45_33475+47del	XP_024308863.1:n.33475+45_33475+47del
XM_024453096.1:c.32908+45_32908+47del	XP_024308864.1:n.32908+45_32908+47del
XM_024453097.1:c.31690+14973_31690+14975del	XP_024308865.1:n.31690+14973_31690+14975del
XM_024453098.1:c.31609+14973_31609+14975del	XP_024308866.1:n.31609+14973_31609+14975del
XM_024453099.1:c.13424-16343_13424-16341del	XP_024308867.1:n.13424-16343_13424-16341del
XM_024453100.1:c.292+45_292+47del	XP_024308868.1:n.292+45_292+47del