Canonical Allele Identifier: CA2504834670

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178786001_178786002insGACCTTGGCAGCAGAAACGTGC , CM000664.2:g.178786001_178786002insGACCTTGGCAGCAGAAACGTGC	GRCh38
NC_000002.11:g.179650728_179650729insGACCTTGGCAGCAGAAACGTGC , CM000664.1:g.179650728_179650729insGACCTTGGCAGCAGAAACGTGC	GRCh37
NC_000002.10:g.179358973_179358974insGACCTTGGCAGCAGAAACGTGC	NCBI36
NG_011618.3:g.49801_49802insGCACGTTTCTGCTGCCAAGGTC , LRG_391:g.49801_49802insGCACGTTTCTGCTGCCAAGGTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	ENSP00000343764.6:p.Arg740HisfsTer16
ENST00000342175.11:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	ENSP00000340554.6:p.Arg694HisfsTer16
ENST00000359218.10:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	ENSP00000352154.5:p.Arg694HisfsTer16
ENST00000360870.10:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC MANE Plus Clinical	ENSP00000354117.4:p.Arg740HisfsTer16
ENST00000342175.10:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	ENSP00000340554.6:p.Arg694HisfsTer16
ENST00000342992.10:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	ENSP00000343764.6:p.Arg740HisfsTer16
ENST00000359218.9:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	ENSP00000352154.5:p.Arg694HisfsTer16
ENST00000360870.9:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	ENSP00000354117.4:p.Arg740HisfsTer16
ENST00000460472.6:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	ENSP00000434586.1:p.Arg694HisfsTer16
ENST00000589042.5:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC MANE Select	ENSP00000467141.1:p.Arg740HisfsTer16
ENST00000591111.5:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	ENSP00000465570.1:p.Arg740HisfsTer16
ENST00000615779.4:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	ENSP00000483597.1:p.Arg740HisfsTer16
NM_001256850.1:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	NP_001243779.1:p.Arg740HisfsTer16
NM_001267550.2:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC MANE Select	NP_001254479.2:p.Arg740HisfsTer16
NM_003319.4:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	NP_003310.4:p.Arg694HisfsTer16
NM_133378.4:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	NP_596869.4:p.Arg740HisfsTer16
NM_133379.4:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC , LRG_391t2:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	NP_596870.2:p.Arg740HisfsTer16
NM_133432.3:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	NP_597676.3:p.Arg694HisfsTer16
NM_133437.4:c.2078_2079insGCACGTTTCTGCTGCCAAGGTC	NP_597681.4:p.Arg694HisfsTer16
XM_011511729.1:c.2264_2265insGCACGTTTCTGCTGCCAAGGTC	XP_011510031.1:p.Arg756HisfsTer16
XM_011511730.1:c.2264_2265insGCACGTTTCTGCTGCCAAGGTC	XP_011510032.1:p.Arg756HisfsTer16
XM_011511731.1:c.2123_2124insGCACGTTTCTGCTGCCAAGGTC	XP_011510033.1:p.Arg709HisfsTer16
XM_011511732.1:c.2261_2262insGCACGTTTCTGCTGCCAAGGTC	XP_011510034.1:p.Arg755HisfsTer16
XM_017004819.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_016860308.1:p.Arg741HisfsTer16
XM_017004820.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_016860309.1:p.Arg741HisfsTer16
XM_017004821.1:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC	XP_016860310.1:p.Arg740HisfsTer16
XM_017004822.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_016860311.1:p.Arg741HisfsTer16
XM_017004823.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_016860312.1:p.Arg741HisfsTer16
XM_024453094.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308862.1:p.Arg741HisfsTer16
XM_024453095.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308863.1:p.Arg741HisfsTer16
XM_024453096.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308864.1:p.Arg741HisfsTer16
XM_024453097.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308865.1:p.Arg741HisfsTer16
XM_024453098.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308866.1:p.Arg741HisfsTer16
XM_024453099.1:c.2219_2220insGCACGTTTCTGCTGCCAAGGTC	XP_024308867.1:p.Arg741HisfsTer16
NM_133379.5:c.2216_2217insGCACGTTTCTGCTGCCAAGGTC MANE Plus Clinical	NP_596870.2:p.Arg740HisfsTer16