Canonical Allele Identifier: CA349610587
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178740485C>G , CM000664.2:g.178740485C>G GRCh38
NC_000002.11:g.179605212C>G , CM000664.1:g.179605212C>G GRCh37
NC_000002.10:g.179313457C>G NCBI36
NG_011618.3:g.95318G>C , LRG_391:g.95318G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.10361-2125G>C ENSP00000343764.6:n.10361-2125G>C
ENST00000342175.11:c.12235G>C ENSP00000340554.6:p.Val4079Leu
ENST00000359218.10:c.12034G>C ENSP00000352154.5:p.Val4012Leu
ENST00000342175.10:c.12235G>C ENSP00000340554.6:p.Val4079Leu
ENST00000342992.10:c.10361-2125G>C ENSP00000343764.6:n.10361-2125G>C
ENST00000359218.9:c.12034G>C ENSP00000352154.5:p.Val4012Leu
ENST00000460472.6:c.11659G>C ENSP00000434586.1:p.Val3887Leu
ENST00000589042.5:c.12748G>C MANE Select ENSP00000467141.1:p.Val4250Leu
ENST00000591111.5:c.11797G>C ENSP00000465570.1:p.Val3933Leu
ENST00000615779.4:c.11797G>C ENSP00000483597.1:p.Val3933Leu
NM_001256850.1:c.11797G>C NP_001243779.1:p.Val3933Leu
NM_001267550.2:c.12748G>C MANE Select NP_001254479.2:p.Val4250Leu
NM_003319.4:c.11659G>C NP_003310.4:p.Val3887Leu
NM_133378.4:c.10361-2125G>C NP_596869.4:n.10361-2125G>C
NM_133432.3:c.12034G>C NP_597676.3:p.Val4012Leu
NM_133437.4:c.12235G>C NP_597681.4:p.Val4079Leu
XM_011511729.1:c.11845G>C XP_011510031.1:p.Val3949Leu
XM_011511730.1:c.11845G>C XP_011510032.1:p.Val3949Leu
XM_011511731.1:c.11704G>C XP_011510033.1:p.Val3902Leu
XM_017004819.1:c.11800G>C XP_016860308.1:p.Val3934Leu
XM_017004820.1:c.10364-2125G>C XP_016860309.1:n.10364-2125G>C
XM_017004821.1:c.10361-2125G>C XP_016860310.1:n.10361-2125G>C
XM_017004822.1:c.11800G>C XP_016860311.1:p.Val3934Leu
XM_017004823.1:c.11800G>C XP_016860312.1:p.Val3934Leu
XM_024453094.1:c.11800G>C XP_024308862.1:p.Val3934Leu
XM_024453095.1:c.11800G>C XP_024308863.1:p.Val3934Leu
XM_024453096.1:c.11800G>C XP_024308864.1:p.Val3934Leu
XM_024453097.1:c.11800G>C XP_024308865.1:p.Val3934Leu
XM_024453098.1:c.11800G>C XP_024308866.1:p.Val3934Leu
XM_024453099.1:c.11800G>C XP_024308867.1:p.Val3934Leu