Canonical Allele Identifier: CA1310544160

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178601535_178601537delinsCTT , CM000664.2:g.178601535_178601537delinsCTT GRCh38
NC_000002.11:g.179466262_179466264delinsCTT , CM000664.1:g.179466262_179466264delinsCTT GRCh37
NC_000002.10:g.179174507_179174509delinsCTT NCBI36
NG_011618.3:g.234266_234268delinsAAG , LRG_391:g.234266_234268delinsAAG
NG_051363.1:g.83709_83711delinsCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.47756_47758delinsAAG (TTN) ENSP00000343764.6:p.Lys15919=
ENST00000342175.11:c.28841_28843delinsAAG (TTN) ENSP00000340554.6:p.Lys9614=
ENST00000359218.10:c.28640_28642delinsAAG (TTN) ENSP00000352154.5:p.Lys9547=
ENST00000342175.10:c.28841_28843delinsAAG (TTN) ENSP00000340554.6:p.Lys9614=
ENST00000342992.10:c.47756_47758delinsAAG (TTN) ENSP00000343764.6:p.Lys15919=
ENST00000359218.9:c.28640_28642delinsAAG (TTN) ENSP00000352154.5:p.Lys9547=
ENST00000460472.6:c.28265_28267delinsAAG (TTN) ENSP00000434586.1:p.Lys9422=
ENST00000589042.5:c.55460_55462delinsAAG (TTN) MANE Select ENSP00000467141.1:p.Lys18487=
ENST00000591111.5:c.50537_50539delinsAAG (TTN) ENSP00000465570.1:p.Lys16846=
ENST00000615779.4:c.50537_50539delinsAAG (TTN) ENSP00000483597.1:p.Lys16846=
NM_001256850.1:c.50537_50539delinsAAG (TTN) NP_001243779.1:p.Lys16846=
NM_001267550.2:c.55460_55462delinsAAG (TTN) MANE Select NP_001254479.2:p.Lys18487=
NM_003319.4:c.28265_28267delinsAAG (TTN) NP_003310.4:p.Lys9422=
NM_133378.4:c.47756_47758delinsAAG (TTN) NP_596869.4:p.Lys15919=
NM_133432.3:c.28640_28642delinsAAG (TTN) NP_597676.3:p.Lys9547=
NM_133437.4:c.28841_28843delinsAAG (TTN) NP_597681.4:p.Lys9614=
NR_038271.1:n.682+3854_682+3856delinsCTT (TTN-AS1)
NR_038272.1:n.3917+868_3917+870delinsCTT (TTN-AS1)
XM_011511729.1:c.54557_54559delinsAAG (TTN) XP_011510031.1:p.Lys18186=
XM_011511730.1:c.28451_28453delinsAAG (TTN) XP_011510032.1:p.Lys9484=
XM_011511731.1:c.28310_28312delinsAAG (TTN) XP_011510033.1:p.Lys9437=
XM_017004819.1:c.54353_54355delinsAAG (TTN) XP_016860308.1:p.Lys18118=
XM_017004820.1:c.49751_49753delinsAAG (TTN) XP_016860309.1:p.Lys16584=
XM_017004821.1:c.49748_49750delinsAAG (TTN) XP_016860310.1:p.Lys16583=
XM_017004822.1:c.46790_46792delinsAAG (TTN) XP_016860311.1:p.Lys15597=
XM_017004823.1:c.28406_28408delinsAAG (TTN) XP_016860312.1:p.Lys9469=
XM_024453094.1:c.49901_49903delinsAAG (TTN) XP_024308862.1:p.Lys16634=
XM_024453095.1:c.49898_49900delinsAAG (TTN) XP_024308863.1:p.Lys16633=
XM_024453096.1:c.49331_49333delinsAAG (TTN) XP_024308864.1:p.Lys16444=
XM_024453097.1:c.46673_46675delinsAAG (TTN) XP_024308865.1:p.Lys15558=
XM_024453098.1:c.46592_46594delinsAAG (TTN) XP_024308866.1:p.Lys15531=
XM_024453099.1:c.28355_28357delinsAAG (TTN) XP_024308867.1:p.Lys9452=
XM_024453100.1:c.18209_18211delinsAAG (TTN) XP_024308868.1:p.Lys6070=