Canonical Allele Identifier: CA1310530873

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178569006T= , CM000664.2:g.178569006T= GRCh38
NC_000002.11:g.179433733T= , CM000664.1:g.179433733T= GRCh37
NC_000002.10:g.179141979T= NCBI36
NG_011618.3:g.266797A= , LRG_391:g.266797A=
NG_051363.1:g.51180T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.69422A= (TTN) ENSP00000343764.6:p.Asp23141=
ENST00000342175.11:c.50507A= (TTN) ENSP00000340554.6:p.Asp16836=
ENST00000359218.10:c.50306A= (TTN) ENSP00000352154.5:p.Asp16769=
ENST00000342175.10:c.50507A= (TTN) ENSP00000340554.6:p.Asp16836=
ENST00000342992.10:c.69422A= (TTN) ENSP00000343764.6:p.Asp23141=
ENST00000359218.9:c.50306A= (TTN) ENSP00000352154.5:p.Asp16769=
ENST00000460472.6:c.49931A= (TTN) ENSP00000434586.1:p.Asp16644=
ENST00000589042.5:c.77126A= (TTN) MANE Select ENSP00000467141.1:p.Asp25709=
ENST00000591111.5:c.72203A= (TTN) ENSP00000465570.1:p.Asp24068=
ENST00000615779.4:c.72203A= (TTN) ENSP00000483597.1:p.Asp24068=
NM_001256850.1:c.72203A= (TTN) NP_001243779.1:p.Asp24068=
NM_001267550.2:c.77126A= (TTN) MANE Select NP_001254479.2:p.Asp25709=
NM_003319.4:c.49931A= (TTN) NP_003310.4:p.Asp16644=
NM_133378.4:c.69422A= (TTN) NP_596869.4:p.Asp23141=
NM_133432.3:c.50306A= (TTN) NP_597676.3:p.Asp16769=
NM_133437.4:c.50507A= (TTN) NP_597681.4:p.Asp16836=
NR_038271.1:n.447-2294T= (TTN-AS1)
NR_038272.1:n.2044-13566T= (TTN-AS1)
XM_011511729.1:c.76223A= (TTN) XP_011510031.1:p.Asp25408=
XM_011511730.1:c.50117A= (TTN) XP_011510032.1:p.Asp16706=
XM_011511731.1:c.49976A= (TTN) XP_011510033.1:p.Asp16659=
XM_017004819.1:c.76019A= (TTN) XP_016860308.1:p.Asp25340=
XM_017004820.1:c.71417A= (TTN) XP_016860309.1:p.Asp23806=
XM_017004821.1:c.71414A= (TTN) XP_016860310.1:p.Asp23805=
XM_017004822.1:c.68456A= (TTN) XP_016860311.1:p.Asp22819=
XM_017004823.1:c.50072A= (TTN) XP_016860312.1:p.Asp16691=
XM_024453094.1:c.71567A= (TTN) XP_024308862.1:p.Asp23856=
XM_024453095.1:c.71564A= (TTN) XP_024308863.1:p.Asp23855=
XM_024453096.1:c.70997A= (TTN) XP_024308864.1:p.Asp23666=
XM_024453097.1:c.68339A= (TTN) XP_024308865.1:p.Asp22780=
XM_024453098.1:c.68258A= (TTN) XP_024308866.1:p.Asp22753=
XM_024453099.1:c.50021A= (TTN) XP_024308867.1:p.Asp16674=
XM_024453100.1:c.39875A= (TTN) XP_024308868.1:p.Asp13292=