Canonical Allele Identifier: CA349647006
Gene: TTN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178631169G>T , CM000664.2:g.178631169G>T GRCh38
NC_000002.11:g.179495896G>T , CM000664.1:g.179495896G>T GRCh37
NC_000002.10:g.179204141G>T NCBI36
NG_011618.3:g.204634C>A , LRG_391:g.204634C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.36175C>A ENSP00000343764.6:p.Pro12059Thr
ENST00000342175.11:c.17260C>A ENSP00000340554.6:p.Pro5754Thr
ENST00000359218.10:c.17059C>A ENSP00000352154.5:p.Pro5687Thr
ENST00000342175.10:c.17260C>A ENSP00000340554.6:p.Pro5754Thr
ENST00000342992.10:c.36175C>A ENSP00000343764.6:p.Pro12059Thr
ENST00000359218.9:c.17059C>A ENSP00000352154.5:p.Pro5687Thr
ENST00000460472.6:c.16684C>A ENSP00000434586.1:p.Pro5562Thr
ENST00000589042.5:c.43879C>A MANE Select ENSP00000467141.1:p.Pro14627Thr
ENST00000591111.5:c.38956C>A ENSP00000465570.1:p.Pro12986Thr
ENST00000615779.4:c.38956C>A ENSP00000483597.1:p.Pro12986Thr
NM_001256850.1:c.38956C>A NP_001243779.1:p.Pro12986Thr
NM_001267550.2:c.43879C>A MANE Select NP_001254479.2:p.Pro14627Thr
NM_003319.4:c.16684C>A NP_003310.4:p.Pro5562Thr
NM_133378.4:c.36175C>A NP_596869.4:p.Pro12059Thr
NM_133432.3:c.17059C>A NP_597676.3:p.Pro5687Thr
NM_133437.4:c.17260C>A NP_597681.4:p.Pro5754Thr
XM_011511729.1:c.42976C>A XP_011510031.1:p.Pro14326Thr
XM_011511730.1:c.16870C>A XP_011510032.1:p.Pro5624Thr
XM_011511731.1:c.16729C>A XP_011510033.1:p.Pro5577Thr
XM_017004819.1:c.42772C>A XP_016860308.1:p.Pro14258Thr
XM_017004820.1:c.38170C>A XP_016860309.1:p.Pro12724Thr
XM_017004821.1:c.38167C>A XP_016860310.1:p.Pro12723Thr
XM_017004822.1:c.35209C>A XP_016860311.1:p.Pro11737Thr
XM_017004823.1:c.16825C>A XP_016860312.1:p.Pro5609Thr
XM_024453094.1:c.38320C>A XP_024308862.1:p.Pro12774Thr
XM_024453095.1:c.38317C>A XP_024308863.1:p.Pro12773Thr
XM_024453096.1:c.37750C>A XP_024308864.1:p.Pro12584Thr
XM_024453097.1:c.35092C>A XP_024308865.1:p.Pro11698Thr
XM_024453098.1:c.35011C>A XP_024308866.1:p.Pro11671Thr
XM_024453099.1:c.16774C>A XP_024308867.1:p.Pro5592Thr
XM_024453100.1:c.6628C>A XP_024308868.1:p.Pro2210Thr