Canonical Allele Identifier: CA1310526770

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559751T= , CM000664.2:g.178559751T= GRCh38
NC_000002.11:g.179424478T= , CM000664.1:g.179424478T= GRCh37
NC_000002.10:g.179132724T= NCBI36
NG_011618.3:g.276052A= , LRG_391:g.276052A=
NG_051363.1:g.41925T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.78677A= (TTN) ENSP00000343764.6:p.Asp26226=
ENST00000342175.11:c.59762A= (TTN) ENSP00000340554.6:p.Asp19921=
ENST00000359218.10:c.59561A= (TTN) ENSP00000352154.5:p.Asp19854=
ENST00000342175.10:c.59762A= (TTN) ENSP00000340554.6:p.Asp19921=
ENST00000342992.10:c.78677A= (TTN) ENSP00000343764.6:p.Asp26226=
ENST00000359218.9:c.59561A= (TTN) ENSP00000352154.5:p.Asp19854=
ENST00000460472.6:c.59186A= (TTN) ENSP00000434586.1:p.Asp19729=
ENST00000589042.5:c.86381A= (TTN) MANE Select ENSP00000467141.1:p.Asp28794=
ENST00000591111.5:c.81458A= (TTN) ENSP00000465570.1:p.Asp27153=
ENST00000615779.4:c.81458A= (TTN) ENSP00000483597.1:p.Asp27153=
NM_001256850.1:c.81458A= (TTN) NP_001243779.1:p.Asp27153=
NM_001267550.2:c.86381A= (TTN) MANE Select NP_001254479.2:p.Asp28794=
NM_003319.4:c.59186A= (TTN) NP_003310.4:p.Asp19729=
NM_133378.4:c.78677A= (TTN) NP_596869.4:p.Asp26226=
NM_133432.3:c.59561A= (TTN) NP_597676.3:p.Asp19854=
NM_133437.4:c.59762A= (TTN) NP_597681.4:p.Asp19921=
NR_038271.1:n.447-11549T= (TTN-AS1)
NR_038272.1:n.2043+17390T= (TTN-AS1)
XM_011511729.1:c.85478A= (TTN) XP_011510031.1:p.Asp28493=
XM_011511730.1:c.59372A= (TTN) XP_011510032.1:p.Asp19791=
XM_011511731.1:c.59231A= (TTN) XP_011510033.1:p.Asp19744=
XM_017004819.1:c.85274A= (TTN) XP_016860308.1:p.Asp28425=
XM_017004820.1:c.80672A= (TTN) XP_016860309.1:p.Asp26891=
XM_017004821.1:c.80669A= (TTN) XP_016860310.1:p.Asp26890=
XM_017004822.1:c.77711A= (TTN) XP_016860311.1:p.Asp25904=
XM_017004823.1:c.59327A= (TTN) XP_016860312.1:p.Asp19776=
XM_024453094.1:c.80822A= (TTN) XP_024308862.1:p.Asp26941=
XM_024453095.1:c.80819A= (TTN) XP_024308863.1:p.Asp26940=
XM_024453096.1:c.80252A= (TTN) XP_024308864.1:p.Asp26751=
XM_024453097.1:c.77594A= (TTN) XP_024308865.1:p.Asp25865=
XM_024453098.1:c.77513A= (TTN) XP_024308866.1:p.Asp25838=
XM_024453099.1:c.59276A= (TTN) XP_024308867.1:p.Asp19759=
XM_024453100.1:c.49130A= (TTN) XP_024308868.1:p.Asp16377=