Canonical Allele Identifier: CA349645555
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178630316A>G , CM000664.2:g.178630316A>G GRCh38
NC_000002.11:g.179495043A>G , CM000664.1:g.179495043A>G GRCh37
NC_000002.10:g.179203288A>G NCBI36
NG_011618.3:g.205487T>C , LRG_391:g.205487T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.36502T>C ENSP00000343764.6:p.Cys12168Arg
ENST00000342175.11:c.17587T>C ENSP00000340554.6:p.Cys5863Arg
ENST00000359218.10:c.17386T>C ENSP00000352154.5:p.Cys5796Arg
ENST00000342175.10:c.17587T>C ENSP00000340554.6:p.Cys5863Arg
ENST00000342992.10:c.36502T>C ENSP00000343764.6:p.Cys12168Arg
ENST00000359218.9:c.17386T>C ENSP00000352154.5:p.Cys5796Arg
ENST00000460472.6:c.17011T>C ENSP00000434586.1:p.Cys5671Arg
ENST00000589042.5:c.44206T>C MANE Select ENSP00000467141.1:p.Cys14736Arg
ENST00000591111.5:c.39283T>C ENSP00000465570.1:p.Cys13095Arg
ENST00000615779.4:c.39283T>C ENSP00000483597.1:p.Cys13095Arg
NM_001256850.1:c.39283T>C NP_001243779.1:p.Cys13095Arg
NM_001267550.2:c.44206T>C MANE Select NP_001254479.2:p.Cys14736Arg
NM_003319.4:c.17011T>C NP_003310.4:p.Cys5671Arg
NM_133378.4:c.36502T>C NP_596869.4:p.Cys12168Arg
NM_133432.3:c.17386T>C NP_597676.3:p.Cys5796Arg
NM_133437.4:c.17587T>C NP_597681.4:p.Cys5863Arg
XM_011511729.1:c.43303T>C XP_011510031.1:p.Cys14435Arg
XM_011511730.1:c.17197T>C XP_011510032.1:p.Cys5733Arg
XM_011511731.1:c.17056T>C XP_011510033.1:p.Cys5686Arg
XM_017004819.1:c.43099T>C XP_016860308.1:p.Cys14367Arg
XM_017004820.1:c.38497T>C XP_016860309.1:p.Cys12833Arg
XM_017004821.1:c.38494T>C XP_016860310.1:p.Cys12832Arg
XM_017004822.1:c.35536T>C XP_016860311.1:p.Cys11846Arg
XM_017004823.1:c.17152T>C XP_016860312.1:p.Cys5718Arg
XM_024453094.1:c.38647T>C XP_024308862.1:p.Cys12883Arg
XM_024453095.1:c.38644T>C XP_024308863.1:p.Cys12882Arg
XM_024453096.1:c.38077T>C XP_024308864.1:p.Cys12693Arg
XM_024453097.1:c.35419T>C XP_024308865.1:p.Cys11807Arg
XM_024453098.1:c.35338T>C XP_024308866.1:p.Cys11780Arg
XM_024453099.1:c.17101T>C XP_024308867.1:p.Cys5701Arg
XM_024453100.1:c.6955T>C XP_024308868.1:p.Cys2319Arg