Canonical Allele Identifier: CA1310530345

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178569325T= , CM000664.2:g.178569325T= GRCh38
NC_000002.11:g.179434052T= , CM000664.1:g.179434052T= GRCh37
NC_000002.10:g.179142298T= NCBI36
NG_011618.3:g.266478A= , LRG_391:g.266478A=
NG_051363.1:g.51499T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69103A= (TTN) ENSP00000343764.6:p.Ser23035=
ENST00000342175.11:c.50188A= (TTN) ENSP00000340554.6:p.Ser16730=
ENST00000359218.10:c.49987A= (TTN) ENSP00000352154.5:p.Ser16663=
ENST00000342175.10:c.50188A= (TTN) ENSP00000340554.6:p.Ser16730=
ENST00000342992.10:c.69103A= (TTN) ENSP00000343764.6:p.Ser23035=
ENST00000359218.9:c.49987A= (TTN) ENSP00000352154.5:p.Ser16663=
ENST00000460472.6:c.49612A= (TTN) ENSP00000434586.1:p.Ser16538=
ENST00000589042.5:c.76807A= (TTN) MANE Select ENSP00000467141.1:p.Ser25603=
ENST00000591111.5:c.71884A= (TTN) ENSP00000465570.1:p.Ser23962=
ENST00000615779.4:c.71884A= (TTN) ENSP00000483597.1:p.Ser23962=
NM_001256850.1:c.71884A= (TTN) NP_001243779.1:p.Ser23962=
NM_001267550.2:c.76807A= (TTN) MANE Select NP_001254479.2:p.Ser25603=
NM_003319.4:c.49612A= (TTN) NP_003310.4:p.Ser16538=
NM_133378.4:c.69103A= (TTN) NP_596869.4:p.Ser23035=
NM_133432.3:c.49987A= (TTN) NP_597676.3:p.Ser16663=
NM_133437.4:c.50188A= (TTN) NP_597681.4:p.Ser16730=
NR_038271.1:n.447-1975T= (TTN-AS1)
NR_038272.1:n.2044-13247T= (TTN-AS1)
XM_011511729.1:c.75904A= (TTN) XP_011510031.1:p.Ser25302=
XM_011511730.1:c.49798A= (TTN) XP_011510032.1:p.Ser16600=
XM_011511731.1:c.49657A= (TTN) XP_011510033.1:p.Ser16553=
XM_017004819.1:c.75700A= (TTN) XP_016860308.1:p.Ser25234=
XM_017004820.1:c.71098A= (TTN) XP_016860309.1:p.Ser23700=
XM_017004821.1:c.71095A= (TTN) XP_016860310.1:p.Ser23699=
XM_017004822.1:c.68137A= (TTN) XP_016860311.1:p.Ser22713=
XM_017004823.1:c.49753A= (TTN) XP_016860312.1:p.Ser16585=
XM_024453094.1:c.71248A= (TTN) XP_024308862.1:p.Ser23750=
XM_024453095.1:c.71245A= (TTN) XP_024308863.1:p.Ser23749=
XM_024453096.1:c.70678A= (TTN) XP_024308864.1:p.Ser23560=
XM_024453097.1:c.68020A= (TTN) XP_024308865.1:p.Ser22674=
XM_024453098.1:c.67939A= (TTN) XP_024308866.1:p.Ser22647=
XM_024453099.1:c.49702A= (TTN) XP_024308867.1:p.Ser16568=
XM_024453100.1:c.39556A= (TTN) XP_024308868.1:p.Ser13186=