Canonical Allele Identifier: CA349645596
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630322G>C , CM000664.2:g.178630322G>C GRCh38
NC_000002.11:g.179495049G>C , CM000664.1:g.179495049G>C GRCh37
NC_000002.10:g.179203294G>C NCBI36
NG_011618.3:g.205481C>G , LRG_391:g.205481C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36496C>G ENSP00000343764.6:p.His12166Asp
ENST00000342175.11:c.17581C>G ENSP00000340554.6:p.His5861Asp
ENST00000359218.10:c.17380C>G ENSP00000352154.5:p.His5794Asp
ENST00000342175.10:c.17581C>G ENSP00000340554.6:p.His5861Asp
ENST00000342992.10:c.36496C>G ENSP00000343764.6:p.His12166Asp
ENST00000359218.9:c.17380C>G ENSP00000352154.5:p.His5794Asp
ENST00000460472.6:c.17005C>G ENSP00000434586.1:p.His5669Asp
ENST00000589042.5:c.44200C>G MANE Select ENSP00000467141.1:p.His14734Asp
ENST00000591111.5:c.39277C>G ENSP00000465570.1:p.His13093Asp
ENST00000615779.4:c.39277C>G ENSP00000483597.1:p.His13093Asp
NM_001256850.1:c.39277C>G NP_001243779.1:p.His13093Asp
NM_001267550.2:c.44200C>G MANE Select NP_001254479.2:p.His14734Asp
NM_003319.4:c.17005C>G NP_003310.4:p.His5669Asp
NM_133378.4:c.36496C>G NP_596869.4:p.His12166Asp
NM_133432.3:c.17380C>G NP_597676.3:p.His5794Asp
NM_133437.4:c.17581C>G NP_597681.4:p.His5861Asp
XM_011511729.1:c.43297C>G XP_011510031.1:p.His14433Asp
XM_011511730.1:c.17191C>G XP_011510032.1:p.His5731Asp
XM_011511731.1:c.17050C>G XP_011510033.1:p.His5684Asp
XM_017004819.1:c.43093C>G XP_016860308.1:p.His14365Asp
XM_017004820.1:c.38491C>G XP_016860309.1:p.His12831Asp
XM_017004821.1:c.38488C>G XP_016860310.1:p.His12830Asp
XM_017004822.1:c.35530C>G XP_016860311.1:p.His11844Asp
XM_017004823.1:c.17146C>G XP_016860312.1:p.His5716Asp
XM_024453094.1:c.38641C>G XP_024308862.1:p.His12881Asp
XM_024453095.1:c.38638C>G XP_024308863.1:p.His12880Asp
XM_024453096.1:c.38071C>G XP_024308864.1:p.His12691Asp
XM_024453097.1:c.35413C>G XP_024308865.1:p.His11805Asp
XM_024453098.1:c.35332C>G XP_024308866.1:p.His11778Asp
XM_024453099.1:c.17095C>G XP_024308867.1:p.His5699Asp
XM_024453100.1:c.6949C>G XP_024308868.1:p.His2317Asp