Canonical Allele Identifier: CA2577173585

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178689470_178689484del , CM000664.2:g.178689470_178689484del	GRCh38
NC_000002.11:g.179554197_179554211del , CM000664.1:g.179554197_179554211del	GRCh37
NC_000002.10:g.179262442_179262456del	NCBI36
NG_011618.3:g.146319_146333del , LRG_391:g.146319_146333del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.28195+31_28195+45del	ENSP00000343764.6:n.28195+31_28195+45del
ENST00000342175.11:c.13859-47167_13859-47153del	ENSP00000340554.6:n.13859-47167_13859-471...
ENST00000359218.10:c.13658-47167_13658-47153del	ENSP00000352154.5:n.13658-47167_13658-471...
ENST00000342175.10:c.13859-47167_13859-47153del	ENSP00000340554.6:n.13859-47167_13859-471...
ENST00000342992.10:c.28195+31_28195+45del	ENSP00000343764.6:n.28195+31_28195+45del
ENST00000359218.9:c.13658-47167_13658-47153del	ENSP00000352154.5:n.13658-47167_13658-471...
ENST00000414766.5:c.1561+31_1561+45del	ENSP00000401501.1:n.1561+31_1561+45del
ENST00000460472.6:c.13283-47167_13283-47153del	ENSP00000434586.1:n.13283-47167_13283-471...
ENST00000589042.5:c.31927+31_31927+45del MANE Select	ENSP00000467141.1:n.31927+31_31927+45del
ENST00000591111.5:c.30976+31_30976+45del	ENSP00000465570.1:n.30976+31_30976+45del
ENST00000615779.4:c.30976+31_30976+45del	ENSP00000483597.1:n.30976+31_30976+45del
NM_001256850.1:c.30976+31_30976+45del	NP_001243779.1:n.30976+31_30976+45del
NM_001267550.2:c.31927+31_31927+45del MANE Select	NP_001254479.2:n.31927+31_31927+45del
NM_003319.4:c.13283-47167_13283-47153del	NP_003310.4:n.13283-47167_13283-47153del
NM_133378.4:c.28195+31_28195+45del	NP_596869.4:n.28195+31_28195+45del
NM_133432.3:c.13658-47167_13658-47153del	NP_597676.3:n.13658-47167_13658-47153del
NM_133437.4:c.13859-47167_13859-47153del	NP_597681.4:n.13859-47167_13859-47153del
XM_011511729.1:c.31024+31_31024+45del	XP_011510031.1:n.31024+31_31024+45del
XM_011511730.1:c.13469-47167_13469-47153del	XP_011510032.1:n.13469-47167_13469-47153d...
XM_011511731.1:c.13328-47167_13328-47153del	XP_011510033.1:n.13328-47167_13328-47153d...
XM_017004819.1:c.30979+31_30979+45del	XP_016860308.1:n.30979+31_30979+45del
XM_017004820.1:c.28198+31_28198+45del	XP_016860309.1:n.28198+31_28198+45del
XM_017004821.1:c.28195+31_28195+45del	XP_016860310.1:n.28195+31_28195+45del
XM_017004822.1:c.30979+31_30979+45del	XP_016860311.1:n.30979+31_30979+45del
XM_017004823.1:c.13424-47167_13424-47153del	XP_016860312.1:n.13424-47167_13424-47153d...
XM_024453094.1:c.30979+31_30979+45del	XP_024308862.1:n.30979+31_30979+45del
XM_024453095.1:c.30979+31_30979+45del	XP_024308863.1:n.30979+31_30979+45del
XM_024453096.1:c.30979+31_30979+45del	XP_024308864.1:n.30979+31_30979+45del
XM_024453097.1:c.30898+329_30898+343del	XP_024308865.1:n.30898+329_30898+343del
XM_024453098.1:c.30898+329_30898+343del	XP_024308866.1:n.30898+329_30898+343del
XM_024453099.1:c.13424-47167_13424-47153del	XP_024308867.1:n.13424-47167_13424-47153d...