Canonical Allele Identifier: CA1310550965

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618224T= , CM000664.2:g.178618224T= GRCh38
NC_000002.11:g.179482951T= , CM000664.1:g.179482951T= GRCh37
NC_000002.10:g.179191196T= NCBI36
NG_011618.3:g.217579A= , LRG_391:g.217579A=
NG_051363.1:g.100398T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.39530A= (TTN) ENSP00000343764.6:p.Glu13177=
ENST00000342175.11:c.20615A= (TTN) ENSP00000340554.6:p.Glu6872=
ENST00000359218.10:c.20414A= (TTN) ENSP00000352154.5:p.Glu6805=
ENST00000342175.10:c.20615A= (TTN) ENSP00000340554.6:p.Glu6872=
ENST00000342992.10:c.39530A= (TTN) ENSP00000343764.6:p.Glu13177=
ENST00000359218.9:c.20414A= (TTN) ENSP00000352154.5:p.Glu6805=
ENST00000460472.6:c.20039A= (TTN) ENSP00000434586.1:p.Glu6680=
ENST00000589042.5:c.47234A= (TTN) MANE Select ENSP00000467141.1:p.Glu15745=
ENST00000591111.5:c.42311A= (TTN) ENSP00000465570.1:p.Glu14104=
ENST00000615779.4:c.42311A= (TTN) ENSP00000483597.1:p.Glu14104=
NM_001256850.1:c.42311A= (TTN) NP_001243779.1:p.Glu14104=
NM_001267550.2:c.47234A= (TTN) MANE Select NP_001254479.2:p.Glu15745=
NM_003319.4:c.20039A= (TTN) NP_003310.4:p.Glu6680=
NM_133378.4:c.39530A= (TTN) NP_596869.4:p.Glu13177=
NM_133432.3:c.20414A= (TTN) NP_597676.3:p.Glu6805=
NM_133437.4:c.20615A= (TTN) NP_597681.4:p.Glu6872=
NR_038271.1:n.1605-1529T= (TTN-AS1)
XM_011511729.1:c.46331A= (TTN) XP_011510031.1:p.Glu15444=
XM_011511730.1:c.20225A= (TTN) XP_011510032.1:p.Glu6742=
XM_011511731.1:c.20084A= (TTN) XP_011510033.1:p.Glu6695=
XM_017004819.1:c.46127A= (TTN) XP_016860308.1:p.Glu15376=
XM_017004820.1:c.41525A= (TTN) XP_016860309.1:p.Glu13842=
XM_017004821.1:c.41522A= (TTN) XP_016860310.1:p.Glu13841=
XM_017004822.1:c.38564A= (TTN) XP_016860311.1:p.Glu12855=
XM_017004823.1:c.20180A= (TTN) XP_016860312.1:p.Glu6727=
XM_024453094.1:c.41675A= (TTN) XP_024308862.1:p.Glu13892=
XM_024453095.1:c.41672A= (TTN) XP_024308863.1:p.Glu13891=
XM_024453096.1:c.41105A= (TTN) XP_024308864.1:p.Glu13702=
XM_024453097.1:c.38447A= (TTN) XP_024308865.1:p.Glu12816=
XM_024453098.1:c.38366A= (TTN) XP_024308866.1:p.Glu12789=
XM_024453099.1:c.20129A= (TTN) XP_024308867.1:p.Glu6710=
XM_024453100.1:c.9983A= (TTN) XP_024308868.1:p.Glu3328=