Canonical Allele Identifier: CA1310537031

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178584479A= , CM000664.2:g.178584479A= GRCh38
NC_000002.11:g.179449206A= , CM000664.1:g.179449206A= GRCh37
NC_000002.10:g.179157452A= NCBI36
NG_011618.3:g.251324T= , LRG_391:g.251324T=
NG_051363.1:g.66653A=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.57368T= (TTN) ENSP00000343764.6:p.Ile19123=
ENST00000342175.11:c.38453T= (TTN) ENSP00000340554.6:p.Ile12818=
ENST00000359218.10:c.38252T= (TTN) ENSP00000352154.5:p.Ile12751=
ENST00000342175.10:c.38453T= (TTN) ENSP00000340554.6:p.Ile12818=
ENST00000342992.10:c.57368T= (TTN) ENSP00000343764.6:p.Ile19123=
ENST00000359218.9:c.38252T= (TTN) ENSP00000352154.5:p.Ile12751=
ENST00000460472.6:c.37877T= (TTN) ENSP00000434586.1:p.Ile12626=
ENST00000589042.5:c.65072T= (TTN) MANE Select ENSP00000467141.1:p.Ile21691=
ENST00000591111.5:c.60149T= (TTN) ENSP00000465570.1:p.Ile20050=
ENST00000615779.4:c.60149T= (TTN) ENSP00000483597.1:p.Ile20050=
NM_001256850.1:c.60149T= (TTN) NP_001243779.1:p.Ile20050=
NM_001267550.2:c.65072T= (TTN) MANE Select NP_001254479.2:p.Ile21691=
NM_003319.4:c.37877T= (TTN) NP_003310.4:p.Ile12626=
NM_133378.4:c.57368T= (TTN) NP_596869.4:p.Ile19123=
NM_133432.3:c.38252T= (TTN) NP_597676.3:p.Ile12751=
NM_133437.4:c.38453T= (TTN) NP_597681.4:p.Ile12818=
NR_038271.1:n.596+13030A= (TTN-AS1)
NR_038272.1:n.2768-94A= (TTN-AS1)
XM_011511729.1:c.64169T= (TTN) XP_011510031.1:p.Ile21390=
XM_011511730.1:c.38063T= (TTN) XP_011510032.1:p.Ile12688=
XM_011511731.1:c.37922T= (TTN) XP_011510033.1:p.Ile12641=
XM_017004819.1:c.63965T= (TTN) XP_016860308.1:p.Ile21322=
XM_017004820.1:c.59363T= (TTN) XP_016860309.1:p.Ile19788=
XM_017004821.1:c.59360T= (TTN) XP_016860310.1:p.Ile19787=
XM_017004822.1:c.56402T= (TTN) XP_016860311.1:p.Ile18801=
XM_017004823.1:c.38018T= (TTN) XP_016860312.1:p.Ile12673=
XM_024453094.1:c.59513T= (TTN) XP_024308862.1:p.Ile19838=
XM_024453095.1:c.59510T= (TTN) XP_024308863.1:p.Ile19837=
XM_024453096.1:c.58943T= (TTN) XP_024308864.1:p.Ile19648=
XM_024453097.1:c.56285T= (TTN) XP_024308865.1:p.Ile18762=
XM_024453098.1:c.56204T= (TTN) XP_024308866.1:p.Ile18735=
XM_024453099.1:c.37967T= (TTN) XP_024308867.1:p.Ile12656=
XM_024453100.1:c.27821T= (TTN) XP_024308868.1:p.Ile9274=