Canonical Allele Identifier: CA1310530970

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178569098C= , CM000664.2:g.178569098C= GRCh38
NC_000002.11:g.179433825C= , CM000664.1:g.179433825C= GRCh37
NC_000002.10:g.179142071C= NCBI36
NG_011618.3:g.266705G= , LRG_391:g.266705G=
NG_051363.1:g.51272C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69330G= (TTN) ENSP00000343764.6:p.Glu23110=
ENST00000342175.11:c.50415G= (TTN) ENSP00000340554.6:p.Glu16805=
ENST00000359218.10:c.50214G= (TTN) ENSP00000352154.5:p.Glu16738=
ENST00000342175.10:c.50415G= (TTN) ENSP00000340554.6:p.Glu16805=
ENST00000342992.10:c.69330G= (TTN) ENSP00000343764.6:p.Glu23110=
ENST00000359218.9:c.50214G= (TTN) ENSP00000352154.5:p.Glu16738=
ENST00000460472.6:c.49839G= (TTN) ENSP00000434586.1:p.Glu16613=
ENST00000589042.5:c.77034G= (TTN) MANE Select ENSP00000467141.1:p.Glu25678=
ENST00000591111.5:c.72111G= (TTN) ENSP00000465570.1:p.Glu24037=
ENST00000615779.4:c.72111G= (TTN) ENSP00000483597.1:p.Glu24037=
NM_001256850.1:c.72111G= (TTN) NP_001243779.1:p.Glu24037=
NM_001267550.2:c.77034G= (TTN) MANE Select NP_001254479.2:p.Glu25678=
NM_003319.4:c.49839G= (TTN) NP_003310.4:p.Glu16613=
NM_133378.4:c.69330G= (TTN) NP_596869.4:p.Glu23110=
NM_133432.3:c.50214G= (TTN) NP_597676.3:p.Glu16738=
NM_133437.4:c.50415G= (TTN) NP_597681.4:p.Glu16805=
NR_038271.1:n.447-2202C= (TTN-AS1)
NR_038272.1:n.2044-13474C= (TTN-AS1)
XM_011511729.1:c.76131G= (TTN) XP_011510031.1:p.Glu25377=
XM_011511730.1:c.50025G= (TTN) XP_011510032.1:p.Glu16675=
XM_011511731.1:c.49884G= (TTN) XP_011510033.1:p.Glu16628=
XM_017004819.1:c.75927G= (TTN) XP_016860308.1:p.Glu25309=
XM_017004820.1:c.71325G= (TTN) XP_016860309.1:p.Glu23775=
XM_017004821.1:c.71322G= (TTN) XP_016860310.1:p.Glu23774=
XM_017004822.1:c.68364G= (TTN) XP_016860311.1:p.Glu22788=
XM_017004823.1:c.49980G= (TTN) XP_016860312.1:p.Glu16660=
XM_024453094.1:c.71475G= (TTN) XP_024308862.1:p.Glu23825=
XM_024453095.1:c.71472G= (TTN) XP_024308863.1:p.Glu23824=
XM_024453096.1:c.70905G= (TTN) XP_024308864.1:p.Glu23635=
XM_024453097.1:c.68247G= (TTN) XP_024308865.1:p.Glu22749=
XM_024453098.1:c.68166G= (TTN) XP_024308866.1:p.Glu22722=
XM_024453099.1:c.49929G= (TTN) XP_024308867.1:p.Glu16643=
XM_024453100.1:c.39783G= (TTN) XP_024308868.1:p.Glu13261=