Canonical Allele Identifier: CA1310579983

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178688963_178688974delinsCAGACCAGATGG , CM000664.2:g.178688963_178688974delinsCAGACCAGATGG	GRCh38
NC_000002.11:g.179553690_179553701delinsCAGACCAGATGG , CM000664.1:g.179553690_179553701delinsCAGACCAGATGG	GRCh37
NC_000002.10:g.179261935_179261946delinsCAGACCAGATGG	NCBI36
NG_011618.3:g.146829_146840delinsCCATCTGGTCTG , LRG_391:g.146829_146840delinsCCATCTGGTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.28363+79_28363+90delinsCCATCTGGTCTG	ENSP00000343764.6:n.28363+79_28363+90delinsCCATCTGGTCTG
ENST00000342175.11:c.13859-46657_13859-46646delinsCCATCTGGTCTG	ENSP00000340554.6:n.13859-46657_13859-46646delinsCCATCTGGTCTG...
ENST00000359218.10:c.13658-46657_13658-46646delinsCCATCTGGTCTG	ENSP00000352154.5:n.13658-46657_13658-46646delinsCCATCTGGTCTG...
ENST00000342175.10:c.13859-46657_13859-46646delinsCCATCTGGTCTG	ENSP00000340554.6:n.13859-46657_13859-46646delinsCCATCTGGTCTG...
ENST00000342992.10:c.28363+79_28363+90delinsCCATCTGGTCTG	ENSP00000343764.6:n.28363+79_28363+90delinsCCATCTGGTCTG
ENST00000359218.9:c.13658-46657_13658-46646delinsCCATCTGGTCTG	ENSP00000352154.5:n.13658-46657_13658-46646delinsCCATCTGGTCTG...
ENST00000414766.5:c.1729+79_1729+90delinsCCATCTGGTCTG	ENSP00000401501.1:n.1729+79_1729+90delinsCCATCTGGTCTG
ENST00000460472.6:c.13283-46657_13283-46646delinsCCATCTGGTCTG	ENSP00000434586.1:n.13283-46657_13283-46646delinsCCATCTGGTCTG...
ENST00000589042.5:c.32095+79_32095+90delinsCCATCTGGTCTG MANE Select	ENSP00000467141.1:n.32095+79_32095+90delinsCCATCTGGTCTG
ENST00000591111.5:c.31144+79_31144+90delinsCCATCTGGTCTG	ENSP00000465570.1:n.31144+79_31144+90delinsCCATCTGGTCTG
ENST00000615779.4:c.31144+79_31144+90delinsCCATCTGGTCTG	ENSP00000483597.1:n.31144+79_31144+90delinsCCATCTGGTCTG
NM_001256850.1:c.31144+79_31144+90delinsCCATCTGGTCTG	NP_001243779.1:n.31144+79_31144+90delinsCCATCTGGTCTG
NM_001267550.2:c.32095+79_32095+90delinsCCATCTGGTCTG MANE Select	NP_001254479.2:n.32095+79_32095+90delinsCCATCTGGTCTG
NM_003319.4:c.13283-46657_13283-46646delinsCCATCTGGTCTG	NP_003310.4:n.13283-46657_13283-46646delinsCCATCTGGTCTG
NM_133378.4:c.28363+79_28363+90delinsCCATCTGGTCTG	NP_596869.4:n.28363+79_28363+90delinsCCATCTGGTCTG
NM_133432.3:c.13658-46657_13658-46646delinsCCATCTGGTCTG	NP_597676.3:n.13658-46657_13658-46646delinsCCATCTGGTCTG
NM_133437.4:c.13859-46657_13859-46646delinsCCATCTGGTCTG	NP_597681.4:n.13859-46657_13859-46646delinsCCATCTGGTCTG
XM_011511729.1:c.31192+79_31192+90delinsCCATCTGGTCTG	XP_011510031.1:n.31192+79_31192+90delinsCCATCTGGTCTG
XM_011511730.1:c.13469-46657_13469-46646delinsCCATCTGGTCTG	XP_011510032.1:n.13469-46657_13469-46646delinsCCATCTGGTCTG
XM_011511731.1:c.13328-46657_13328-46646delinsCCATCTGGTCTG	XP_011510033.1:n.13328-46657_13328-46646delinsCCATCTGGTCTG
XM_017004819.1:c.31147+79_31147+90delinsCCATCTGGTCTG	XP_016860308.1:n.31147+79_31147+90delinsCCATCTGGTCTG
XM_017004820.1:c.28366+79_28366+90delinsCCATCTGGTCTG	XP_016860309.1:n.28366+79_28366+90delinsCCATCTGGTCTG
XM_017004821.1:c.28363+79_28363+90delinsCCATCTGGTCTG	XP_016860310.1:n.28363+79_28363+90delinsCCATCTGGTCTG
XM_017004822.1:c.31147+79_31147+90delinsCCATCTGGTCTG	XP_016860311.1:n.31147+79_31147+90delinsCCATCTGGTCTG
XM_017004823.1:c.13424-46657_13424-46646delinsCCATCTGGTCTG	XP_016860312.1:n.13424-46657_13424-46646delinsCCATCTGGTCTG
XM_024453094.1:c.31147+79_31147+90delinsCCATCTGGTCTG	XP_024308862.1:n.31147+79_31147+90delinsCCATCTGGTCTG
XM_024453095.1:c.31147+79_31147+90delinsCCATCTGGTCTG	XP_024308863.1:n.31147+79_31147+90delinsCCATCTGGTCTG
XM_024453096.1:c.31147+79_31147+90delinsCCATCTGGTCTG	XP_024308864.1:n.31147+79_31147+90delinsCCATCTGGTCTG
XM_024453097.1:c.30898+839_30898+850delinsCCATCTGGTCTG	XP_024308865.1:n.30898+839_30898+850delinsCCATCTGGTCTG
XM_024453098.1:c.30898+839_30898+850delinsCCATCTGGTCTG	XP_024308866.1:n.30898+839_30898+850delinsCCATCTGGTCTG
XM_024453099.1:c.13424-46657_13424-46646delinsCCATCTGGTCTG	XP_024308867.1:n.13424-46657_13424-46646delinsCCATCTGGTCTG