Canonical Allele Identifier: CA349645531
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630312C>G , CM000664.2:g.178630312C>G GRCh38
NC_000002.11:g.179495039C>G , CM000664.1:g.179495039C>G GRCh37
NC_000002.10:g.179203284C>G NCBI36
NG_011618.3:g.205491G>C , LRG_391:g.205491G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36506G>C ENSP00000343764.6:p.Arg12169Pro
ENST00000342175.11:c.17591G>C ENSP00000340554.6:p.Arg5864Pro
ENST00000359218.10:c.17390G>C ENSP00000352154.5:p.Arg5797Pro
ENST00000342175.10:c.17591G>C ENSP00000340554.6:p.Arg5864Pro
ENST00000342992.10:c.36506G>C ENSP00000343764.6:p.Arg12169Pro
ENST00000359218.9:c.17390G>C ENSP00000352154.5:p.Arg5797Pro
ENST00000460472.6:c.17015G>C ENSP00000434586.1:p.Arg5672Pro
ENST00000589042.5:c.44210G>C MANE Select ENSP00000467141.1:p.Arg14737Pro
ENST00000591111.5:c.39287G>C ENSP00000465570.1:p.Arg13096Pro
ENST00000615779.4:c.39287G>C ENSP00000483597.1:p.Arg13096Pro
NM_001256850.1:c.39287G>C NP_001243779.1:p.Arg13096Pro
NM_001267550.2:c.44210G>C MANE Select NP_001254479.2:p.Arg14737Pro
NM_003319.4:c.17015G>C NP_003310.4:p.Arg5672Pro
NM_133378.4:c.36506G>C NP_596869.4:p.Arg12169Pro
NM_133432.3:c.17390G>C NP_597676.3:p.Arg5797Pro
NM_133437.4:c.17591G>C NP_597681.4:p.Arg5864Pro
XM_011511729.1:c.43307G>C XP_011510031.1:p.Arg14436Pro
XM_011511730.1:c.17201G>C XP_011510032.1:p.Arg5734Pro
XM_011511731.1:c.17060G>C XP_011510033.1:p.Arg5687Pro
XM_017004819.1:c.43103G>C XP_016860308.1:p.Arg14368Pro
XM_017004820.1:c.38501G>C XP_016860309.1:p.Arg12834Pro
XM_017004821.1:c.38498G>C XP_016860310.1:p.Arg12833Pro
XM_017004822.1:c.35540G>C XP_016860311.1:p.Arg11847Pro
XM_017004823.1:c.17156G>C XP_016860312.1:p.Arg5719Pro
XM_024453094.1:c.38651G>C XP_024308862.1:p.Arg12884Pro
XM_024453095.1:c.38648G>C XP_024308863.1:p.Arg12883Pro
XM_024453096.1:c.38081G>C XP_024308864.1:p.Arg12694Pro
XM_024453097.1:c.35423G>C XP_024308865.1:p.Arg11808Pro
XM_024453098.1:c.35342G>C XP_024308866.1:p.Arg11781Pro
XM_024453099.1:c.17105G>C XP_024308867.1:p.Arg5702Pro
XM_024453100.1:c.6959G>C XP_024308868.1:p.Arg2320Pro