Canonical Allele Identifier: CA1310521556

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178544381C= , CM000664.2:g.178544381C= GRCh38
NC_000002.11:g.179409108C= , CM000664.1:g.179409108C= GRCh37
NC_000002.10:g.179117354C= NCBI36
NG_011618.3:g.291422G= , LRG_391:g.291422G=
NG_051363.1:g.26555C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.88144G= (TTN) ENSP00000343764.6:p.Glu29382=
ENST00000342175.11:c.69229G= (TTN) ENSP00000340554.6:p.Glu23077=
ENST00000359218.10:c.69028G= (TTN) ENSP00000352154.5:p.Glu23010=
ENST00000342175.10:c.69229G= (TTN) ENSP00000340554.6:p.Glu23077=
ENST00000342992.10:c.88144G= (TTN) ENSP00000343764.6:p.Glu29382=
ENST00000359218.9:c.69028G= (TTN) ENSP00000352154.5:p.Glu23010=
ENST00000460472.6:c.68653G= (TTN) ENSP00000434586.1:p.Glu22885=
ENST00000589042.5:c.95848G= (TTN) MANE Select ENSP00000467141.1:p.Glu31950=
ENST00000591111.5:c.90925G= (TTN) ENSP00000465570.1:p.Glu30309=
ENST00000615779.4:c.90925G= (TTN) ENSP00000483597.1:p.Glu30309=
NM_001256850.1:c.90925G= (TTN) NP_001243779.1:p.Glu30309=
NM_001267550.2:c.95848G= (TTN) MANE Select NP_001254479.2:p.Glu31950=
NM_003319.4:c.68653G= (TTN) NP_003310.4:p.Glu22885=
NM_133378.4:c.88144G= (TTN) NP_596869.4:p.Glu29382=
NM_133432.3:c.69028G= (TTN) NP_597676.3:p.Glu23010=
NM_133437.4:c.69229G= (TTN) NP_597681.4:p.Glu23077=
NR_038271.1:n.446+20745C= (TTN-AS1)
NR_038272.1:n.2043+2020C= (TTN-AS1)
XM_011511729.1:c.94945G= (TTN) XP_011510031.1:p.Glu31649=
XM_011511730.1:c.68839G= (TTN) XP_011510032.1:p.Glu22947=
XM_011511731.1:c.68698G= (TTN) XP_011510033.1:p.Glu22900=
XM_017004819.1:c.94741G= (TTN) XP_016860308.1:p.Glu31581=
XM_017004820.1:c.90139G= (TTN) XP_016860309.1:p.Glu30047=
XM_017004821.1:c.90136G= (TTN) XP_016860310.1:p.Glu30046=
XM_017004822.1:c.87178G= (TTN) XP_016860311.1:p.Glu29060=
XM_017004823.1:c.68794G= (TTN) XP_016860312.1:p.Glu22932=
XM_024453094.1:c.90289G= (TTN) XP_024308862.1:p.Glu30097=
XM_024453095.1:c.90286G= (TTN) XP_024308863.1:p.Glu30096=
XM_024453096.1:c.89719G= (TTN) XP_024308864.1:p.Glu29907=
XM_024453097.1:c.87061G= (TTN) XP_024308865.1:p.Glu29021=
XM_024453098.1:c.86980G= (TTN) XP_024308866.1:p.Glu28994=
XM_024453099.1:c.68743G= (TTN) XP_024308867.1:p.Glu22915=
XM_024453100.1:c.58597G= (TTN) XP_024308868.1:p.Glu19533=