Canonical Allele Identifier: CA1310518107

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178532160A= , CM000664.2:g.178532160A= GRCh38
NC_000002.11:g.179396887A= , CM000664.1:g.179396887A= GRCh37
NC_000002.10:g.179105133A= NCBI36
NG_011618.3:g.303643T= , LRG_391:g.303643T=
NG_051363.1:g.14334A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.96751T= (TTN) ENSP00000343764.6:p.Tyr32251=
ENST00000342175.11:c.77836T= (TTN) ENSP00000340554.6:p.Tyr25946=
ENST00000359218.10:c.77635T= (TTN) ENSP00000352154.5:p.Tyr25879=
ENST00000342175.10:c.77836T= (TTN) ENSP00000340554.6:p.Tyr25946=
ENST00000342992.10:c.96751T= (TTN) ENSP00000343764.6:p.Tyr32251=
ENST00000359218.9:c.77635T= (TTN) ENSP00000352154.5:p.Tyr25879=
ENST00000460472.6:c.77260T= (TTN) ENSP00000434586.1:p.Tyr25754=
ENST00000589042.5:c.104455T= (TTN) MANE Select ENSP00000467141.1:p.Tyr34819=
ENST00000591111.5:c.99532T= (TTN) ENSP00000465570.1:p.Tyr33178=
ENST00000615779.4:c.99532T= (TTN) ENSP00000483597.1:p.Tyr33178=
NM_001256850.1:c.99532T= (TTN) NP_001243779.1:p.Tyr33178=
NM_001267550.2:c.104455T= (TTN) MANE Select NP_001254479.2:p.Tyr34819=
NM_003319.4:c.77260T= (TTN) NP_003310.4:p.Tyr25754=
NM_133378.4:c.96751T= (TTN) NP_596869.4:p.Tyr32251=
NM_133432.3:c.77635T= (TTN) NP_597676.3:p.Tyr25879=
NM_133437.4:c.77836T= (TTN) NP_597681.4:p.Tyr25946=
NR_038271.1:n.446+8524A= (TTN-AS1)
NR_038272.1:n.220-3572A= (TTN-AS1)
XM_011511729.1:c.103552T= (TTN) XP_011510031.1:p.Tyr34518=
XM_011511730.1:c.77446T= (TTN) XP_011510032.1:p.Tyr25816=
XM_011511731.1:c.77305T= (TTN) XP_011510033.1:p.Tyr25769=
XM_017004819.1:c.103348T= (TTN) XP_016860308.1:p.Tyr34450=
XM_017004820.1:c.98746T= (TTN) XP_016860309.1:p.Tyr32916=
XM_017004821.1:c.98743T= (TTN) XP_016860310.1:p.Tyr32915=
XM_017004822.1:c.95785T= (TTN) XP_016860311.1:p.Tyr31929=
XM_017004823.1:c.77401T= (TTN) XP_016860312.1:p.Tyr25801=
XM_024453094.1:c.98896T= (TTN) XP_024308862.1:p.Tyr32966=
XM_024453095.1:c.98893T= (TTN) XP_024308863.1:p.Tyr32965=
XM_024453096.1:c.98326T= (TTN) XP_024308864.1:p.Tyr32776=
XM_024453097.1:c.95668T= (TTN) XP_024308865.1:p.Tyr31890=
XM_024453098.1:c.95587T= (TTN) XP_024308866.1:p.Tyr31863=
XM_024453099.1:c.77350T= (TTN) XP_024308867.1:p.Tyr25784=
XM_024453100.1:c.67204T= (TTN) XP_024308868.1:p.Tyr22402=