Canonical Allele Identifier: CA1310508279

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527602T= , CM000664.2:g.178527602T= GRCh38
NC_000002.11:g.179392329T= , CM000664.1:g.179392329T= GRCh37
NC_000002.10:g.179100575T= NCBI36
NG_011618.3:g.308201A= , LRG_391:g.308201A=
NG_051363.1:g.9776T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.99820A= (TTN) ENSP00000343764.6:p.Ser33274=
ENST00000342175.11:c.80905A= (TTN) ENSP00000340554.6:p.Ser26969=
ENST00000359218.10:c.80704A= (TTN) ENSP00000352154.5:p.Ser26902=
ENST00000342175.10:c.80905A= (TTN) ENSP00000340554.6:p.Ser26969=
ENST00000342992.10:c.99820A= (TTN) ENSP00000343764.6:p.Ser33274=
ENST00000359218.9:c.80704A= (TTN) ENSP00000352154.5:p.Ser26902=
ENST00000460472.6:c.80329A= (TTN) ENSP00000434586.1:p.Ser26777=
ENST00000589042.5:c.107524A= (TTN) MANE Select ENSP00000467141.1:p.Ser35842=
ENST00000591111.5:c.102601A= (TTN) ENSP00000465570.1:p.Ser34201=
ENST00000615779.4:c.102601A= (TTN) ENSP00000483597.1:p.Ser34201=
NM_001256850.1:c.102601A= (TTN) NP_001243779.1:p.Ser34201=
NM_001267550.2:c.107524A= (TTN) MANE Select NP_001254479.2:p.Ser35842=
NM_003319.4:c.80329A= (TTN) NP_003310.4:p.Ser26777=
NM_133378.4:c.99820A= (TTN) NP_596869.4:p.Ser33274=
NM_133432.3:c.80704A= (TTN) NP_597676.3:p.Ser26902=
NM_133437.4:c.80905A= (TTN) NP_597681.4:p.Ser26969=
NR_038271.1:n.446+3966T= (TTN-AS1)
NR_038272.1:n.219+3966T= (TTN-AS1)
XM_011511729.1:c.106621A= (TTN) XP_011510031.1:p.Ser35541=
XM_011511730.1:c.80515A= (TTN) XP_011510032.1:p.Ser26839=
XM_011511731.1:c.80374A= (TTN) XP_011510033.1:p.Ser26792=
XM_017004819.1:c.106417A= (TTN) XP_016860308.1:p.Ser35473=
XM_017004820.1:c.101815A= (TTN) XP_016860309.1:p.Ser33939=
XM_017004821.1:c.101812A= (TTN) XP_016860310.1:p.Ser33938=
XM_017004822.1:c.98854A= (TTN) XP_016860311.1:p.Ser32952=
XM_017004823.1:c.80470A= (TTN) XP_016860312.1:p.Ser26824=
XM_024453094.1:c.101965A= (TTN) XP_024308862.1:p.Ser33989=
XM_024453095.1:c.101962A= (TTN) XP_024308863.1:p.Ser33988=
XM_024453096.1:c.101395A= (TTN) XP_024308864.1:p.Ser33799=
XM_024453097.1:c.98737A= (TTN) XP_024308865.1:p.Ser32913=
XM_024453098.1:c.98656A= (TTN) XP_024308866.1:p.Ser32886=
XM_024453099.1:c.80419A= (TTN) XP_024308867.1:p.Ser26807=
XM_024453100.1:c.70273A= (TTN) XP_024308868.1:p.Ser23425=