Canonical Allele Identifier: CA1310539678

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178590939A= , CM000664.2:g.178590939A= GRCh38
NC_000002.11:g.179455666A= , CM000664.1:g.179455666A= GRCh37
NC_000002.10:g.179163912A= NCBI36
NG_011618.3:g.244864T= , LRG_391:g.244864T=
NG_051363.1:g.73113A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.53082T= (TTN) ENSP00000343764.6:p.Pro17694=
ENST00000342175.11:c.34167T= (TTN) ENSP00000340554.6:p.Pro11389=
ENST00000359218.10:c.33966T= (TTN) ENSP00000352154.5:p.Pro11322=
ENST00000342175.10:c.34167T= (TTN) ENSP00000340554.6:p.Pro11389=
ENST00000342992.10:c.53082T= (TTN) ENSP00000343764.6:p.Pro17694=
ENST00000359218.9:c.33966T= (TTN) ENSP00000352154.5:p.Pro11322=
ENST00000460472.6:c.33591T= (TTN) ENSP00000434586.1:p.Pro11197=
ENST00000589042.5:c.60786T= (TTN) MANE Select ENSP00000467141.1:p.Pro20262=
ENST00000591111.5:c.55863T= (TTN) ENSP00000465570.1:p.Pro18621=
ENST00000615779.4:c.55863T= (TTN) ENSP00000483597.1:p.Pro18621=
NM_001256850.1:c.55863T= (TTN) NP_001243779.1:p.Pro18621=
NM_001267550.2:c.60786T= (TTN) MANE Select NP_001254479.2:p.Pro20262=
NM_003319.4:c.33591T= (TTN) NP_003310.4:p.Pro11197=
NM_133378.4:c.53082T= (TTN) NP_596869.4:p.Pro17694=
NM_133432.3:c.33966T= (TTN) NP_597676.3:p.Pro11322=
NM_133437.4:c.34167T= (TTN) NP_597681.4:p.Pro11389=
NR_038271.1:n.597-6657A= (TTN-AS1)
NR_038272.1:n.3189-200A= (TTN-AS1)
XM_011511729.1:c.59883T= (TTN) XP_011510031.1:p.Pro19961=
XM_011511730.1:c.33777T= (TTN) XP_011510032.1:p.Pro11259=
XM_011511731.1:c.33636T= (TTN) XP_011510033.1:p.Pro11212=
XM_017004819.1:c.59679T= (TTN) XP_016860308.1:p.Pro19893=
XM_017004820.1:c.55077T= (TTN) XP_016860309.1:p.Pro18359=
XM_017004821.1:c.55074T= (TTN) XP_016860310.1:p.Pro18358=
XM_017004822.1:c.52116T= (TTN) XP_016860311.1:p.Pro17372=
XM_017004823.1:c.33732T= (TTN) XP_016860312.1:p.Pro11244=
XM_024453094.1:c.55227T= (TTN) XP_024308862.1:p.Pro18409=
XM_024453095.1:c.55224T= (TTN) XP_024308863.1:p.Pro18408=
XM_024453096.1:c.54657T= (TTN) XP_024308864.1:p.Pro18219=
XM_024453097.1:c.51999T= (TTN) XP_024308865.1:p.Pro17333=
XM_024453098.1:c.51918T= (TTN) XP_024308866.1:p.Pro17306=
XM_024453099.1:c.33681T= (TTN) XP_024308867.1:p.Pro11227=
XM_024453100.1:c.23535T= (TTN) XP_024308868.1:p.Pro7845=