Canonical Allele Identifier: CA349640259
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178624497T>C , CM000664.2:g.178624497T>C GRCh38
NC_000002.11:g.179489224T>C , CM000664.1:g.179489224T>C GRCh37
NC_000002.10:g.179197469T>C NCBI36
NG_011618.3:g.211306A>G , LRG_391:g.211306A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.37079A>G ENSP00000343764.6:p.Asp12360Gly
ENST00000342175.11:c.18164A>G ENSP00000340554.6:p.Asp6055Gly
ENST00000359218.10:c.17963A>G ENSP00000352154.5:p.Asp5988Gly
ENST00000342175.10:c.18164A>G ENSP00000340554.6:p.Asp6055Gly
ENST00000342992.10:c.37079A>G ENSP00000343764.6:p.Asp12360Gly
ENST00000359218.9:c.17963A>G ENSP00000352154.5:p.Asp5988Gly
ENST00000460472.6:c.17588A>G ENSP00000434586.1:p.Asp5863Gly
ENST00000589042.5:c.44783A>G MANE Select ENSP00000467141.1:p.Asp14928Gly
ENST00000591111.5:c.39860A>G ENSP00000465570.1:p.Asp13287Gly
ENST00000615779.4:c.39860A>G ENSP00000483597.1:p.Asp13287Gly
NM_001256850.1:c.39860A>G NP_001243779.1:p.Asp13287Gly
NM_001267550.2:c.44783A>G MANE Select NP_001254479.2:p.Asp14928Gly
NM_003319.4:c.17588A>G NP_003310.4:p.Asp5863Gly
NM_133378.4:c.37079A>G NP_596869.4:p.Asp12360Gly
NM_133432.3:c.17963A>G NP_597676.3:p.Asp5988Gly
NM_133437.4:c.18164A>G NP_597681.4:p.Asp6055Gly
XM_011511729.1:c.43880A>G XP_011510031.1:p.Asp14627Gly
XM_011511730.1:c.17774A>G XP_011510032.1:p.Asp5925Gly
XM_011511731.1:c.17633A>G XP_011510033.1:p.Asp5878Gly
XM_017004819.1:c.43676A>G XP_016860308.1:p.Asp14559Gly
XM_017004820.1:c.39074A>G XP_016860309.1:p.Asp13025Gly
XM_017004821.1:c.39071A>G XP_016860310.1:p.Asp13024Gly
XM_017004822.1:c.36113A>G XP_016860311.1:p.Asp12038Gly
XM_017004823.1:c.17729A>G XP_016860312.1:p.Asp5910Gly
XM_024453094.1:c.39224A>G XP_024308862.1:p.Asp13075Gly
XM_024453095.1:c.39221A>G XP_024308863.1:p.Asp13074Gly
XM_024453096.1:c.38654A>G XP_024308864.1:p.Asp12885Gly
XM_024453097.1:c.35996A>G XP_024308865.1:p.Asp11999Gly
XM_024453098.1:c.35915A>G XP_024308866.1:p.Asp11972Gly
XM_024453099.1:c.17678A>G XP_024308867.1:p.Asp5893Gly
XM_024453100.1:c.7532A>G XP_024308868.1:p.Asp2511Gly