Canonical Allele Identifier: CA1310540002

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178592703C= , CM000664.2:g.178592703C= GRCh38
NC_000002.11:g.179457430C= , CM000664.1:g.179457430C= GRCh37
NC_000002.10:g.179165676C= NCBI36
NG_011618.3:g.243100G= , LRG_391:g.243100G=
NG_051363.1:g.74877C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.51641-43G= (TTN) ENSP00000343764.6:n.51641-43G=
ENST00000342175.11:c.32726-43G= (TTN) ENSP00000340554.6:n.32726-43G=
ENST00000359218.10:c.32525-43G= (TTN) ENSP00000352154.5:n.32525-43G=
ENST00000342175.10:c.32726-43G= (TTN) ENSP00000340554.6:n.32726-43G=
ENST00000342992.10:c.51641-43G= (TTN) ENSP00000343764.6:n.51641-43G=
ENST00000359218.9:c.32525-43G= (TTN) ENSP00000352154.5:n.32525-43G=
ENST00000460472.6:c.32150-43G= (TTN) ENSP00000434586.1:n.32150-43G=
ENST00000589042.5:c.59345-43G= (TTN) MANE Select ENSP00000467141.1:n.59345-43G=
ENST00000591111.5:c.54422-43G= (TTN) ENSP00000465570.1:n.54422-43G=
ENST00000615779.4:c.54422-43G= (TTN) ENSP00000483597.1:n.54422-43G=
NM_001256850.1:c.54422-43G= (TTN) NP_001243779.1:n.54422-43G=
NM_001267550.2:c.59345-43G= (TTN) MANE Select NP_001254479.2:n.59345-43G=
NM_003319.4:c.32150-43G= (TTN) NP_003310.4:n.32150-43G=
NM_133378.4:c.51641-43G= (TTN) NP_596869.4:n.51641-43G=
NM_133432.3:c.32525-43G= (TTN) NP_597676.3:n.32525-43G=
NM_133437.4:c.32726-43G= (TTN) NP_597681.4:n.32726-43G=
NR_038271.1:n.597-4893C= (TTN-AS1)
NR_038272.1:n.3364+1389C= (TTN-AS1)
XM_011511729.1:c.58442-43G= (TTN) XP_011510031.1:n.58442-43G=
XM_011511730.1:c.32336-43G= (TTN) XP_011510032.1:n.32336-43G=
XM_011511731.1:c.32195-43G= (TTN) XP_011510033.1:n.32195-43G=
XM_017004819.1:c.58238-43G= (TTN) XP_016860308.1:n.58238-43G=
XM_017004820.1:c.53636-43G= (TTN) XP_016860309.1:n.53636-43G=
XM_017004821.1:c.53633-43G= (TTN) XP_016860310.1:n.53633-43G=
XM_017004822.1:c.50675-43G= (TTN) XP_016860311.1:n.50675-43G=
XM_017004823.1:c.32291-43G= (TTN) XP_016860312.1:n.32291-43G=
XM_024453094.1:c.53786-43G= (TTN) XP_024308862.1:n.53786-43G=
XM_024453095.1:c.53783-43G= (TTN) XP_024308863.1:n.53783-43G=
XM_024453096.1:c.53216-43G= (TTN) XP_024308864.1:n.53216-43G=
XM_024453097.1:c.50558-43G= (TTN) XP_024308865.1:n.50558-43G=
XM_024453098.1:c.50477-43G= (TTN) XP_024308866.1:n.50477-43G=
XM_024453099.1:c.32240-43G= (TTN) XP_024308867.1:n.32240-43G=
XM_024453100.1:c.22094-43G= (TTN) XP_024308868.1:n.22094-43G=