Canonical Allele Identifier: CA349634733
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178621310C>G , CM000664.2:g.178621310C>G GRCh38
NC_000002.11:g.179486037C>G , CM000664.1:g.179486037C>G GRCh37
NC_000002.10:g.179194282C>G NCBI36
NG_011618.3:g.214493G>C , LRG_391:g.214493G>C
NG_051363.1:g.103484C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.37704G>C ENSP00000343764.6:p.Lys12568Asn
ENST00000342175.11:c.18789G>C ENSP00000340554.6:p.Lys6263Asn
ENST00000359218.10:c.18588G>C ENSP00000352154.5:p.Lys6196Asn
ENST00000342175.10:c.18789G>C ENSP00000340554.6:p.Lys6263Asn
ENST00000342992.10:c.37704G>C ENSP00000343764.6:p.Lys12568Asn
ENST00000359218.9:c.18588G>C ENSP00000352154.5:p.Lys6196Asn
ENST00000460472.6:c.18213G>C ENSP00000434586.1:p.Lys6071Asn
ENST00000589042.5:c.45408G>C MANE Select ENSP00000467141.1:p.Lys15136Asn
ENST00000591111.5:c.40485G>C ENSP00000465570.1:p.Lys13495Asn
ENST00000615779.4:c.40485G>C ENSP00000483597.1:p.Lys13495Asn
NM_001256850.1:c.40485G>C NP_001243779.1:p.Lys13495Asn
NM_001267550.2:c.45408G>C MANE Select NP_001254479.2:p.Lys15136Asn
NM_003319.4:c.18213G>C NP_003310.4:p.Lys6071Asn
NM_133378.4:c.37704G>C NP_596869.4:p.Lys12568Asn
NM_133432.3:c.18588G>C NP_597676.3:p.Lys6196Asn
NM_133437.4:c.18789G>C NP_597681.4:p.Lys6263Asn
XM_011511729.1:c.44505G>C XP_011510031.1:p.Lys14835Asn
XM_011511730.1:c.18399G>C XP_011510032.1:p.Lys6133Asn
XM_011511731.1:c.18258G>C XP_011510033.1:p.Lys6086Asn
XM_017004819.1:c.44301G>C XP_016860308.1:p.Lys14767Asn
XM_017004820.1:c.39699G>C XP_016860309.1:p.Lys13233Asn
XM_017004821.1:c.39696G>C XP_016860310.1:p.Lys13232Asn
XM_017004822.1:c.36738G>C XP_016860311.1:p.Lys12246Asn
XM_017004823.1:c.18354G>C XP_016860312.1:p.Lys6118Asn
XM_024453094.1:c.39849G>C XP_024308862.1:p.Lys13283Asn
XM_024453095.1:c.39846G>C XP_024308863.1:p.Lys13282Asn
XM_024453096.1:c.39279G>C XP_024308864.1:p.Lys13093Asn
XM_024453097.1:c.36621G>C XP_024308865.1:p.Lys12207Asn
XM_024453098.1:c.36540G>C XP_024308866.1:p.Lys12180Asn
XM_024453099.1:c.18303G>C XP_024308867.1:p.Lys6101Asn
XM_024453100.1:c.8157G>C XP_024308868.1:p.Lys2719Asn