Canonical Allele Identifier: CA430286687
Community Standard Title: NM_001267550.2(TTN):c.24390T>C (p.Asp8130=)
Gene: TTN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178718810A>G , CM000664.2:g.178718810A>G GRCh38
NC_000002.11:g.179583537A>G , CM000664.1:g.179583537A>G GRCh37
NC_000002.10:g.179291782A>G NCBI36
NG_011618.3:g.116993T>C , LRG_391:g.116993T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001267550.2:c.24390T>C MANE Select NP_001254479.2:p.Asp8130=
ENST00000589042.5:c.24390T>C MANE Select ENSP00000467141.1:p.Asp8130=
NM_001256850.1:c.23439T>C NP_001243779.1:p.Asp7813=
NM_003319.4:c.13282+19272T>C NP_003310.4:n.13282+19272T>C
NM_133378.4:c.20658T>C NP_596869.4:p.Asp6886=
NM_133432.3:c.13657+19272T>C NP_597676.3:n.13657+19272T>C
NM_133437.4:c.13858+19272T>C NP_597681.4:n.13858+19272T>C
ENST00000342175.10:c.13858+19272T>C ENSP00000340554.6:n.13858+19272T>C
ENST00000342175.11:c.13858+19272T>C ENSP00000340554.6:n.13858+19272T>C
ENST00000342992.10:c.20658T>C ENSP00000343764.6:p.Asp6886=
ENST00000342992.11:c.20658T>C ENSP00000343764.6:p.Asp6886=
ENST00000359218.10:c.13657+19272T>C ENSP00000352154.5:n.13657+19272T>C
ENST00000359218.9:c.13657+19272T>C ENSP00000352154.5:n.13657+19272T>C
ENST00000460472.6:c.13282+19272T>C ENSP00000434586.1:n.13282+19272T>C
ENST00000591111.5:c.23439T>C ENSP00000465570.1:p.Asp7813=
ENST00000615779.4:c.23439T>C ENSP00000483597.1:p.Asp7813=
XM_011511729.1:c.23487T>C XP_011510031.1:p.Asp7829=
XM_011511730.1:c.13468+19272T>C XP_011510032.1:n.13468+19272T>C
XM_011511731.1:c.13327+19272T>C XP_011510033.1:n.13327+19272T>C
XM_017004819.1:c.23442T>C XP_016860308.1:p.Asp7814=
XM_017004820.1:c.20661T>C XP_016860309.1:p.Asp6887=
XM_017004821.1:c.20658T>C XP_016860310.1:p.Asp6886=
XM_017004822.1:c.23442T>C XP_016860311.1:p.Asp7814=
XM_017004823.1:c.13423+19272T>C XP_016860312.1:n.13423+19272T>C
XM_024453094.1:c.23442T>C XP_024308862.1:p.Asp7814=
XM_024453095.1:c.23442T>C XP_024308863.1:p.Asp7814=
XM_024453096.1:c.23442T>C XP_024308864.1:p.Asp7814=
XM_024453097.1:c.23442T>C XP_024308865.1:p.Asp7814=
XM_024453098.1:c.23442T>C XP_024308866.1:p.Asp7814=
XM_024453099.1:c.13423+19272T>C XP_024308867.1:n.13423+19272T>C