Canonical Allele Identifier: CA349645584
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630320G>C , CM000664.2:g.178630320G>C GRCh38
NC_000002.11:g.179495047G>C , CM000664.1:g.179495047G>C GRCh37
NC_000002.10:g.179203292G>C NCBI36
NG_011618.3:g.205483C>G , LRG_391:g.205483C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36498C>G ENSP00000343764.6:p.His12166Gln
ENST00000342175.11:c.17583C>G ENSP00000340554.6:p.His5861Gln
ENST00000359218.10:c.17382C>G ENSP00000352154.5:p.His5794Gln
ENST00000342175.10:c.17583C>G ENSP00000340554.6:p.His5861Gln
ENST00000342992.10:c.36498C>G ENSP00000343764.6:p.His12166Gln
ENST00000359218.9:c.17382C>G ENSP00000352154.5:p.His5794Gln
ENST00000460472.6:c.17007C>G ENSP00000434586.1:p.His5669Gln
ENST00000589042.5:c.44202C>G MANE Select ENSP00000467141.1:p.His14734Gln
ENST00000591111.5:c.39279C>G ENSP00000465570.1:p.His13093Gln
ENST00000615779.4:c.39279C>G ENSP00000483597.1:p.His13093Gln
NM_001256850.1:c.39279C>G NP_001243779.1:p.His13093Gln
NM_001267550.2:c.44202C>G MANE Select NP_001254479.2:p.His14734Gln
NM_003319.4:c.17007C>G NP_003310.4:p.His5669Gln
NM_133378.4:c.36498C>G NP_596869.4:p.His12166Gln
NM_133432.3:c.17382C>G NP_597676.3:p.His5794Gln
NM_133437.4:c.17583C>G NP_597681.4:p.His5861Gln
XM_011511729.1:c.43299C>G XP_011510031.1:p.His14433Gln
XM_011511730.1:c.17193C>G XP_011510032.1:p.His5731Gln
XM_011511731.1:c.17052C>G XP_011510033.1:p.His5684Gln
XM_017004819.1:c.43095C>G XP_016860308.1:p.His14365Gln
XM_017004820.1:c.38493C>G XP_016860309.1:p.His12831Gln
XM_017004821.1:c.38490C>G XP_016860310.1:p.His12830Gln
XM_017004822.1:c.35532C>G XP_016860311.1:p.His11844Gln
XM_017004823.1:c.17148C>G XP_016860312.1:p.His5716Gln
XM_024453094.1:c.38643C>G XP_024308862.1:p.His12881Gln
XM_024453095.1:c.38640C>G XP_024308863.1:p.His12880Gln
XM_024453096.1:c.38073C>G XP_024308864.1:p.His12691Gln
XM_024453097.1:c.35415C>G XP_024308865.1:p.His11805Gln
XM_024453098.1:c.35334C>G XP_024308866.1:p.His11778Gln
XM_024453099.1:c.17097C>G XP_024308867.1:p.His5699Gln
XM_024453100.1:c.6951C>G XP_024308868.1:p.His2317Gln