Canonical Allele Identifier: CA2577172406

Gene: TTN

Linked Data

• gnomAD v4: 2-178658697-ATACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178658703_178658706del , CM000664.2:g.178658703_178658706del	GRCh38
NC_000002.11:g.179523430_179523433del , CM000664.1:g.179523430_179523433del	GRCh37
NC_000002.10:g.179231675_179231678del	NCBI36
NG_011618.3:g.177102_177105del , LRG_391:g.177102_177105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.31741+304_31741+307del	ENSP00000343764.6:n.31741+304_31741+307del
ENST00000342175.11:c.13859-16384_13859-16381del	ENSP00000340554.6:n.13859-16384_13859-16381del
ENST00000359218.10:c.13658-16384_13658-16381del	ENSP00000352154.5:n.13658-16384_13658-16381del
ENST00000342175.10:c.13859-16384_13859-16381del	ENSP00000340554.6:n.13859-16384_13859-16381del
ENST00000342992.10:c.31741+304_31741+307del	ENSP00000343764.6:n.31741+304_31741+307del
ENST00000359218.9:c.13658-16384_13658-16381del	ENSP00000352154.5:n.13658-16384_13658-16381del
ENST00000414766.5:c.2440+14932_2440+14935del	ENSP00000401501.1:n.2440+14932_2440+14935del
ENST00000460472.6:c.13283-16384_13283-16381del	ENSP00000434586.1:n.13283-16384_13283-16381del
ENST00000589042.5:c.37543+4_37543+7del
ENST00000591111.5:c.34354+4_34354+7del
ENST00000615779.4:c.34522+304_34522+307del	ENSP00000483597.1:n.34522+304_34522+307del
NM_001256850.1:c.34522+304_34522+307del	NP_001243779.1:n.34522+304_34522+307del
NM_001267550.2:c.37543+4_37543+7del
NM_003319.4:c.13283-16384_13283-16381del	NP_003310.4:n.13283-16384_13283-16381del
NM_133378.4:c.31741+304_31741+307del	NP_596869.4:n.31741+304_31741+307del
NM_133432.3:c.13658-16384_13658-16381del	NP_597676.3:n.13658-16384_13658-16381del
NM_133437.4:c.13859-16384_13859-16381del	NP_597681.4:n.13859-16384_13859-16381del
XM_011511729.1:c.36640+4_36640+7del
XM_011511730.1:c.13469-16384_13469-16381del	XP_011510032.1:n.13469-16384_13469-16381del
XM_011511731.1:c.13328-16384_13328-16381del	XP_011510033.1:n.13328-16384_13328-16381del
XM_017004819.1:c.36436+4_36436+7del
XM_017004820.1:c.31834+4_31834+7del
XM_017004821.1:c.31831+4_31831+7del
XM_017004822.1:c.31858+14932_31858+14935del	XP_016860311.1:n.31858+14932_31858+14935del
XM_017004823.1:c.13424-16384_13424-16381del	XP_016860312.1:n.13424-16384_13424-16381del
XM_024453094.1:c.33478+4_33478+7del
XM_024453095.1:c.33475+4_33475+7del
XM_024453096.1:c.32908+4_32908+7del
XM_024453097.1:c.31690+14932_31690+14935del	XP_024308865.1:n.31690+14932_31690+14935del
XM_024453098.1:c.31609+14932_31609+14935del	XP_024308866.1:n.31609+14932_31609+14935del
XM_024453099.1:c.13424-16384_13424-16381del	XP_024308867.1:n.13424-16384_13424-16381del
XM_024453100.1:c.292+4_292+7del