Canonical Allele Identifier: CA349641099
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178624681C>G , CM000664.2:g.178624681C>G GRCh38
NC_000002.11:g.179489408C>G , CM000664.1:g.179489408C>G GRCh37
NC_000002.10:g.179197653C>G NCBI36
NG_011618.3:g.211122G>C , LRG_391:g.211122G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36895G>C ENSP00000343764.6:p.Gly12299Arg
ENST00000342175.11:c.17980G>C ENSP00000340554.6:p.Gly5994Arg
ENST00000359218.10:c.17779G>C ENSP00000352154.5:p.Gly5927Arg
ENST00000342175.10:c.17980G>C ENSP00000340554.6:p.Gly5994Arg
ENST00000342992.10:c.36895G>C ENSP00000343764.6:p.Gly12299Arg
ENST00000359218.9:c.17779G>C ENSP00000352154.5:p.Gly5927Arg
ENST00000460472.6:c.17404G>C ENSP00000434586.1:p.Gly5802Arg
ENST00000589042.5:c.44599G>C MANE Select ENSP00000467141.1:p.Gly14867Arg
ENST00000591111.5:c.39676G>C ENSP00000465570.1:p.Gly13226Arg
ENST00000615779.4:c.39676G>C ENSP00000483597.1:p.Gly13226Arg
NM_001256850.1:c.39676G>C NP_001243779.1:p.Gly13226Arg
NM_001267550.2:c.44599G>C MANE Select NP_001254479.2:p.Gly14867Arg
NM_003319.4:c.17404G>C NP_003310.4:p.Gly5802Arg
NM_133378.4:c.36895G>C NP_596869.4:p.Gly12299Arg
NM_133432.3:c.17779G>C NP_597676.3:p.Gly5927Arg
NM_133437.4:c.17980G>C NP_597681.4:p.Gly5994Arg
XM_011511729.1:c.43696G>C XP_011510031.1:p.Gly14566Arg
XM_011511730.1:c.17590G>C XP_011510032.1:p.Gly5864Arg
XM_011511731.1:c.17449G>C XP_011510033.1:p.Gly5817Arg
XM_017004819.1:c.43492G>C XP_016860308.1:p.Gly14498Arg
XM_017004820.1:c.38890G>C XP_016860309.1:p.Gly12964Arg
XM_017004821.1:c.38887G>C XP_016860310.1:p.Gly12963Arg
XM_017004822.1:c.35929G>C XP_016860311.1:p.Gly11977Arg
XM_017004823.1:c.17545G>C XP_016860312.1:p.Gly5849Arg
XM_024453094.1:c.39040G>C XP_024308862.1:p.Gly13014Arg
XM_024453095.1:c.39037G>C XP_024308863.1:p.Gly13013Arg
XM_024453096.1:c.38470G>C XP_024308864.1:p.Gly12824Arg
XM_024453097.1:c.35812G>C XP_024308865.1:p.Gly11938Arg
XM_024453098.1:c.35731G>C XP_024308866.1:p.Gly11911Arg
XM_024453099.1:c.17494G>C XP_024308867.1:p.Gly5832Arg
XM_024453100.1:c.7348G>C XP_024308868.1:p.Gly2450Arg