Canonical Allele Identifier: CA349602499
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178738221G>C , CM000664.2:g.178738221G>C GRCh38
NC_000002.11:g.179602948G>C , CM000664.1:g.179602948G>C GRCh37
NC_000002.10:g.179311193G>C NCBI36
NG_011618.3:g.97582C>G , LRG_391:g.97582C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.10500C>G ENSP00000343764.6:p.Asp3500Glu
ENST00000342175.11:c.13719C>G ENSP00000340554.6:p.Asp4573Glu
ENST00000359218.10:c.13518C>G ENSP00000352154.5:p.Asp4506Glu
ENST00000342175.10:c.13719C>G ENSP00000340554.6:p.Asp4573Glu
ENST00000342992.10:c.10500C>G ENSP00000343764.6:p.Asp3500Glu
ENST00000359218.9:c.13518C>G ENSP00000352154.5:p.Asp4506Glu
ENST00000460472.6:c.13143C>G ENSP00000434586.1:p.Asp4381Glu
ENST00000589042.5:c.14232C>G MANE Select ENSP00000467141.1:p.Asp4744Glu
ENST00000591111.5:c.13281C>G ENSP00000465570.1:p.Asp4427Glu
ENST00000615779.4:c.13281C>G ENSP00000483597.1:p.Asp4427Glu
NM_001256850.1:c.13281C>G NP_001243779.1:p.Asp4427Glu
NM_001267550.2:c.14232C>G MANE Select NP_001254479.2:p.Asp4744Glu
NM_003319.4:c.13143C>G NP_003310.4:p.Asp4381Glu
NM_133378.4:c.10500C>G NP_596869.4:p.Asp3500Glu
NM_133432.3:c.13518C>G NP_597676.3:p.Asp4506Glu
NM_133437.4:c.13719C>G NP_597681.4:p.Asp4573Glu
XM_011511729.1:c.13329C>G XP_011510031.1:p.Asp4443Glu
XM_011511730.1:c.13329C>G XP_011510032.1:p.Asp4443Glu
XM_011511731.1:c.13188C>G XP_011510033.1:p.Asp4396Glu
XM_017004819.1:c.13284C>G XP_016860308.1:p.Asp4428Glu
XM_017004820.1:c.10503C>G XP_016860309.1:p.Asp3501Glu
XM_017004821.1:c.10500C>G XP_016860310.1:p.Asp3500Glu
XM_017004822.1:c.13284C>G XP_016860311.1:p.Asp4428Glu
XM_017004823.1:c.13284C>G XP_016860312.1:p.Asp4428Glu
XM_024453094.1:c.13284C>G XP_024308862.1:p.Asp4428Glu
XM_024453095.1:c.13284C>G XP_024308863.1:p.Asp4428Glu
XM_024453096.1:c.13284C>G XP_024308864.1:p.Asp4428Glu
XM_024453097.1:c.13284C>G XP_024308865.1:p.Asp4428Glu
XM_024453098.1:c.13284C>G XP_024308866.1:p.Asp4428Glu
XM_024453099.1:c.13284C>G XP_024308867.1:p.Asp4428Glu