Canonical Allele Identifier: CA1310532238

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178573867T= , CM000664.2:g.178573867T= GRCh38
NC_000002.11:g.179438594T= , CM000664.1:g.179438594T= GRCh37
NC_000002.10:g.179146840T= NCBI36
NG_011618.3:g.261936A= , LRG_391:g.261936A=
NG_051363.1:g.56041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.64561A= (TTN) ENSP00000343764.6:p.Asn21521=
ENST00000342175.11:c.45646A= (TTN) ENSP00000340554.6:p.Asn15216=
ENST00000359218.10:c.45445A= (TTN) ENSP00000352154.5:p.Asn15149=
ENST00000342175.10:c.45646A= (TTN) ENSP00000340554.6:p.Asn15216=
ENST00000342992.10:c.64561A= (TTN) ENSP00000343764.6:p.Asn21521=
ENST00000359218.9:c.45445A= (TTN) ENSP00000352154.5:p.Asn15149=
ENST00000460472.6:c.45070A= (TTN) ENSP00000434586.1:p.Asn15024=
ENST00000589042.5:c.72265A= (TTN) MANE Select ENSP00000467141.1:p.Asn24089=
ENST00000591111.5:c.67342A= (TTN) ENSP00000465570.1:p.Asn22448=
ENST00000615779.4:c.67342A= (TTN) ENSP00000483597.1:p.Asn22448=
NM_001256850.1:c.67342A= (TTN) NP_001243779.1:p.Asn22448=
NM_001267550.2:c.72265A= (TTN) MANE Select NP_001254479.2:p.Asn24089=
NM_003319.4:c.45070A= (TTN) NP_003310.4:p.Asn15024=
NM_133378.4:c.64561A= (TTN) NP_596869.4:p.Asn21521=
NM_133432.3:c.45445A= (TTN) NP_597676.3:p.Asn15149=
NM_133437.4:c.45646A= (TTN) NP_597681.4:p.Asn15216=
NR_038271.1:n.596+2418T= (TTN-AS1)
NR_038272.1:n.2044-8705T= (TTN-AS1)
XM_011511729.1:c.71362A= (TTN) XP_011510031.1:p.Asn23788=
XM_011511730.1:c.45256A= (TTN) XP_011510032.1:p.Asn15086=
XM_011511731.1:c.45115A= (TTN) XP_011510033.1:p.Asn15039=
XM_017004819.1:c.71158A= (TTN) XP_016860308.1:p.Asn23720=
XM_017004820.1:c.66556A= (TTN) XP_016860309.1:p.Asn22186=
XM_017004821.1:c.66553A= (TTN) XP_016860310.1:p.Asn22185=
XM_017004822.1:c.63595A= (TTN) XP_016860311.1:p.Asn21199=
XM_017004823.1:c.45211A= (TTN) XP_016860312.1:p.Asn15071=
XM_024453094.1:c.66706A= (TTN) XP_024308862.1:p.Asn22236=
XM_024453095.1:c.66703A= (TTN) XP_024308863.1:p.Asn22235=
XM_024453096.1:c.66136A= (TTN) XP_024308864.1:p.Asn22046=
XM_024453097.1:c.63478A= (TTN) XP_024308865.1:p.Asn21160=
XM_024453098.1:c.63397A= (TTN) XP_024308866.1:p.Asn21133=
XM_024453099.1:c.45160A= (TTN) XP_024308867.1:p.Asn15054=
XM_024453100.1:c.35014A= (TTN) XP_024308868.1:p.Asn11672=