Canonical Allele Identifier: CA1310530967

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178569097T= , CM000664.2:g.178569097T= GRCh38
NC_000002.11:g.179433824T= , CM000664.1:g.179433824T= GRCh37
NC_000002.10:g.179142070T= NCBI36
NG_011618.3:g.266706A= , LRG_391:g.266706A=
NG_051363.1:g.51271T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69331A= (TTN) ENSP00000343764.6:p.Asn23111=
ENST00000342175.11:c.50416A= (TTN) ENSP00000340554.6:p.Asn16806=
ENST00000359218.10:c.50215A= (TTN) ENSP00000352154.5:p.Asn16739=
ENST00000342175.10:c.50416A= (TTN) ENSP00000340554.6:p.Asn16806=
ENST00000342992.10:c.69331A= (TTN) ENSP00000343764.6:p.Asn23111=
ENST00000359218.9:c.50215A= (TTN) ENSP00000352154.5:p.Asn16739=
ENST00000460472.6:c.49840A= (TTN) ENSP00000434586.1:p.Asn16614=
ENST00000589042.5:c.77035A= (TTN) MANE Select ENSP00000467141.1:p.Asn25679=
ENST00000591111.5:c.72112A= (TTN) ENSP00000465570.1:p.Asn24038=
ENST00000615779.4:c.72112A= (TTN) ENSP00000483597.1:p.Asn24038=
NM_001256850.1:c.72112A= (TTN) NP_001243779.1:p.Asn24038=
NM_001267550.2:c.77035A= (TTN) MANE Select NP_001254479.2:p.Asn25679=
NM_003319.4:c.49840A= (TTN) NP_003310.4:p.Asn16614=
NM_133378.4:c.69331A= (TTN) NP_596869.4:p.Asn23111=
NM_133432.3:c.50215A= (TTN) NP_597676.3:p.Asn16739=
NM_133437.4:c.50416A= (TTN) NP_597681.4:p.Asn16806=
NR_038271.1:n.447-2203T= (TTN-AS1)
NR_038272.1:n.2044-13475T= (TTN-AS1)
XM_011511729.1:c.76132A= (TTN) XP_011510031.1:p.Asn25378=
XM_011511730.1:c.50026A= (TTN) XP_011510032.1:p.Asn16676=
XM_011511731.1:c.49885A= (TTN) XP_011510033.1:p.Asn16629=
XM_017004819.1:c.75928A= (TTN) XP_016860308.1:p.Asn25310=
XM_017004820.1:c.71326A= (TTN) XP_016860309.1:p.Asn23776=
XM_017004821.1:c.71323A= (TTN) XP_016860310.1:p.Asn23775=
XM_017004822.1:c.68365A= (TTN) XP_016860311.1:p.Asn22789=
XM_017004823.1:c.49981A= (TTN) XP_016860312.1:p.Asn16661=
XM_024453094.1:c.71476A= (TTN) XP_024308862.1:p.Asn23826=
XM_024453095.1:c.71473A= (TTN) XP_024308863.1:p.Asn23825=
XM_024453096.1:c.70906A= (TTN) XP_024308864.1:p.Asn23636=
XM_024453097.1:c.68248A= (TTN) XP_024308865.1:p.Asn22750=
XM_024453098.1:c.68167A= (TTN) XP_024308866.1:p.Asn22723=
XM_024453099.1:c.49930A= (TTN) XP_024308867.1:p.Asn16644=
XM_024453100.1:c.39784A= (TTN) XP_024308868.1:p.Asn13262=