Canonical Allele Identifier: CA1310523143

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178546522A= , CM000664.2:g.178546522A= GRCh38
NC_000002.11:g.179411249A= , CM000664.1:g.179411249A= GRCh37
NC_000002.10:g.179119495A= NCBI36
NG_011618.3:g.289281T= , LRG_391:g.289281T=
NG_051363.1:g.28696A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.87125-20T= (TTN) ENSP00000343764.6:n.87125-20T=
ENST00000342175.11:c.68210-20T= (TTN) ENSP00000340554.6:n.68210-20T=
ENST00000359218.10:c.68009-20T= (TTN) ENSP00000352154.5:n.68009-20T=
ENST00000342175.10:c.68210-20T= (TTN) ENSP00000340554.6:n.68210-20T=
ENST00000342992.10:c.87125-20T= (TTN) ENSP00000343764.6:n.87125-20T=
ENST00000359218.9:c.68009-20T= (TTN) ENSP00000352154.5:n.68009-20T=
ENST00000460472.6:c.67634-20T= (TTN) ENSP00000434586.1:n.67634-20T=
ENST00000589042.5:c.94829-20T= (TTN) MANE Select ENSP00000467141.1:n.94829-20T=
ENST00000591111.5:c.89906-20T= (TTN) ENSP00000465570.1:n.89906-20T=
ENST00000615779.4:c.89906-20T= (TTN) ENSP00000483597.1:n.89906-20T=
NM_001256850.1:c.89906-20T= (TTN) NP_001243779.1:n.89906-20T=
NM_001267550.2:c.94829-20T= (TTN) MANE Select NP_001254479.2:n.94829-20T=
NM_003319.4:c.67634-20T= (TTN) NP_003310.4:n.67634-20T=
NM_133378.4:c.87125-20T= (TTN) NP_596869.4:n.87125-20T=
NM_133432.3:c.68009-20T= (TTN) NP_597676.3:n.68009-20T=
NM_133437.4:c.68210-20T= (TTN) NP_597681.4:n.68210-20T=
NR_038271.1:n.446+22886A= (TTN-AS1)
NR_038272.1:n.2043+4161A= (TTN-AS1)
XM_011511729.1:c.93926-20T= (TTN) XP_011510031.1:n.93926-20T=
XM_011511730.1:c.67820-20T= (TTN) XP_011510032.1:n.67820-20T=
XM_011511731.1:c.67679-20T= (TTN) XP_011510033.1:n.67679-20T=
XM_017004819.1:c.93722-20T= (TTN) XP_016860308.1:n.93722-20T=
XM_017004820.1:c.89120-20T= (TTN) XP_016860309.1:n.89120-20T=
XM_017004821.1:c.89117-20T= (TTN) XP_016860310.1:n.89117-20T=
XM_017004822.1:c.86159-20T= (TTN) XP_016860311.1:n.86159-20T=
XM_017004823.1:c.67775-20T= (TTN) XP_016860312.1:n.67775-20T=
XM_024453094.1:c.89270-20T= (TTN) XP_024308862.1:n.89270-20T=
XM_024453095.1:c.89267-20T= (TTN) XP_024308863.1:n.89267-20T=
XM_024453096.1:c.88700-20T= (TTN) XP_024308864.1:n.88700-20T=
XM_024453097.1:c.86042-20T= (TTN) XP_024308865.1:n.86042-20T=
XM_024453098.1:c.85961-20T= (TTN) XP_024308866.1:n.85961-20T=
XM_024453099.1:c.67724-20T= (TTN) XP_024308867.1:n.67724-20T=
XM_024453100.1:c.57578-20T= (TTN) XP_024308868.1:n.57578-20T=