Canonical Allele Identifier: CA349645590
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630321T>C , CM000664.2:g.178630321T>C GRCh38
NC_000002.11:g.179495048T>C , CM000664.1:g.179495048T>C GRCh37
NC_000002.10:g.179203293T>C NCBI36
NG_011618.3:g.205482A>G , LRG_391:g.205482A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36497A>G ENSP00000343764.6:p.His12166Arg
ENST00000342175.11:c.17582A>G ENSP00000340554.6:p.His5861Arg
ENST00000359218.10:c.17381A>G ENSP00000352154.5:p.His5794Arg
ENST00000342175.10:c.17582A>G ENSP00000340554.6:p.His5861Arg
ENST00000342992.10:c.36497A>G ENSP00000343764.6:p.His12166Arg
ENST00000359218.9:c.17381A>G ENSP00000352154.5:p.His5794Arg
ENST00000460472.6:c.17006A>G ENSP00000434586.1:p.His5669Arg
ENST00000589042.5:c.44201A>G MANE Select ENSP00000467141.1:p.His14734Arg
ENST00000591111.5:c.39278A>G ENSP00000465570.1:p.His13093Arg
ENST00000615779.4:c.39278A>G ENSP00000483597.1:p.His13093Arg
NM_001256850.1:c.39278A>G NP_001243779.1:p.His13093Arg
NM_001267550.2:c.44201A>G MANE Select NP_001254479.2:p.His14734Arg
NM_003319.4:c.17006A>G NP_003310.4:p.His5669Arg
NM_133378.4:c.36497A>G NP_596869.4:p.His12166Arg
NM_133432.3:c.17381A>G NP_597676.3:p.His5794Arg
NM_133437.4:c.17582A>G NP_597681.4:p.His5861Arg
XM_011511729.1:c.43298A>G XP_011510031.1:p.His14433Arg
XM_011511730.1:c.17192A>G XP_011510032.1:p.His5731Arg
XM_011511731.1:c.17051A>G XP_011510033.1:p.His5684Arg
XM_017004819.1:c.43094A>G XP_016860308.1:p.His14365Arg
XM_017004820.1:c.38492A>G XP_016860309.1:p.His12831Arg
XM_017004821.1:c.38489A>G XP_016860310.1:p.His12830Arg
XM_017004822.1:c.35531A>G XP_016860311.1:p.His11844Arg
XM_017004823.1:c.17147A>G XP_016860312.1:p.His5716Arg
XM_024453094.1:c.38642A>G XP_024308862.1:p.His12881Arg
XM_024453095.1:c.38639A>G XP_024308863.1:p.His12880Arg
XM_024453096.1:c.38072A>G XP_024308864.1:p.His12691Arg
XM_024453097.1:c.35414A>G XP_024308865.1:p.His11805Arg
XM_024453098.1:c.35333A>G XP_024308866.1:p.His11778Arg
XM_024453099.1:c.17096A>G XP_024308867.1:p.His5699Arg
XM_024453100.1:c.6950A>G XP_024308868.1:p.His2317Arg