Canonical Allele Identifier: CA1310522188

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178545482A= , CM000664.2:g.178545482A= GRCh38
NC_000002.11:g.179410209A= , CM000664.1:g.179410209A= GRCh37
NC_000002.10:g.179118455A= NCBI36
NG_011618.3:g.290321T= , LRG_391:g.290321T=
NG_051363.1:g.27656A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.87924T= (TTN) ENSP00000343764.6:p.Gly29308=
ENST00000342175.11:c.69009T= (TTN) ENSP00000340554.6:p.Gly23003=
ENST00000359218.10:c.68808T= (TTN) ENSP00000352154.5:p.Gly22936=
ENST00000342175.10:c.69009T= (TTN) ENSP00000340554.6:p.Gly23003=
ENST00000342992.10:c.87924T= (TTN) ENSP00000343764.6:p.Gly29308=
ENST00000359218.9:c.68808T= (TTN) ENSP00000352154.5:p.Gly22936=
ENST00000460472.6:c.68433T= (TTN) ENSP00000434586.1:p.Gly22811=
ENST00000589042.5:c.95628T= (TTN) MANE Select ENSP00000467141.1:p.Gly31876=
ENST00000591111.5:c.90705T= (TTN) ENSP00000465570.1:p.Gly30235=
ENST00000615779.4:c.90705T= (TTN) ENSP00000483597.1:p.Gly30235=
NM_001256850.1:c.90705T= (TTN) NP_001243779.1:p.Gly30235=
NM_001267550.2:c.95628T= (TTN) MANE Select NP_001254479.2:p.Gly31876=
NM_003319.4:c.68433T= (TTN) NP_003310.4:p.Gly22811=
NM_133378.4:c.87924T= (TTN) NP_596869.4:p.Gly29308=
NM_133432.3:c.68808T= (TTN) NP_597676.3:p.Gly22936=
NM_133437.4:c.69009T= (TTN) NP_597681.4:p.Gly23003=
NR_038271.1:n.446+21846A= (TTN-AS1)
NR_038272.1:n.2043+3121A= (TTN-AS1)
XM_011511729.1:c.94725T= (TTN) XP_011510031.1:p.Gly31575=
XM_011511730.1:c.68619T= (TTN) XP_011510032.1:p.Gly22873=
XM_011511731.1:c.68478T= (TTN) XP_011510033.1:p.Gly22826=
XM_017004819.1:c.94521T= (TTN) XP_016860308.1:p.Gly31507=
XM_017004820.1:c.89919T= (TTN) XP_016860309.1:p.Gly29973=
XM_017004821.1:c.89916T= (TTN) XP_016860310.1:p.Gly29972=
XM_017004822.1:c.86958T= (TTN) XP_016860311.1:p.Gly28986=
XM_017004823.1:c.68574T= (TTN) XP_016860312.1:p.Gly22858=
XM_024453094.1:c.90069T= (TTN) XP_024308862.1:p.Gly30023=
XM_024453095.1:c.90066T= (TTN) XP_024308863.1:p.Gly30022=
XM_024453096.1:c.89499T= (TTN) XP_024308864.1:p.Gly29833=
XM_024453097.1:c.86841T= (TTN) XP_024308865.1:p.Gly28947=
XM_024453098.1:c.86760T= (TTN) XP_024308866.1:p.Gly28920=
XM_024453099.1:c.68523T= (TTN) XP_024308867.1:p.Gly22841=
XM_024453100.1:c.58377T= (TTN) XP_024308868.1:p.Gly19459=