Canonical Allele Identifier: CA1310537076

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178584567C= , CM000664.2:g.178584567C= GRCh38
NC_000002.11:g.179449294C= , CM000664.1:g.179449294C= GRCh37
NC_000002.10:g.179157540C= NCBI36
NG_011618.3:g.251236G= , LRG_391:g.251236G=
NG_051363.1:g.66741C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.57280G= (TTN) ENSP00000343764.6:p.Glu19094=
ENST00000342175.11:c.38365G= (TTN) ENSP00000340554.6:p.Glu12789=
ENST00000359218.10:c.38164G= (TTN) ENSP00000352154.5:p.Glu12722=
ENST00000342175.10:c.38365G= (TTN) ENSP00000340554.6:p.Glu12789=
ENST00000342992.10:c.57280G= (TTN) ENSP00000343764.6:p.Glu19094=
ENST00000359218.9:c.38164G= (TTN) ENSP00000352154.5:p.Glu12722=
ENST00000460472.6:c.37789G= (TTN) ENSP00000434586.1:p.Glu12597=
ENST00000589042.5:c.64984G= (TTN) MANE Select ENSP00000467141.1:p.Glu21662=
ENST00000591111.5:c.60061G= (TTN) ENSP00000465570.1:p.Glu20021=
ENST00000615779.4:c.60061G= (TTN) ENSP00000483597.1:p.Glu20021=
NM_001256850.1:c.60061G= (TTN) NP_001243779.1:p.Glu20021=
NM_001267550.2:c.64984G= (TTN) MANE Select NP_001254479.2:p.Glu21662=
NM_003319.4:c.37789G= (TTN) NP_003310.4:p.Glu12597=
NM_133378.4:c.57280G= (TTN) NP_596869.4:p.Glu19094=
NM_133432.3:c.38164G= (TTN) NP_597676.3:p.Glu12722=
NM_133437.4:c.38365G= (TTN) NP_597681.4:p.Glu12789=
NR_038271.1:n.597-13029C= (TTN-AS1)
NR_038272.1:n.2768-6C= (TTN-AS1)
XM_011511729.1:c.64081G= (TTN) XP_011510031.1:p.Glu21361=
XM_011511730.1:c.37975G= (TTN) XP_011510032.1:p.Glu12659=
XM_011511731.1:c.37834G= (TTN) XP_011510033.1:p.Glu12612=
XM_017004819.1:c.63877G= (TTN) XP_016860308.1:p.Glu21293=
XM_017004820.1:c.59275G= (TTN) XP_016860309.1:p.Glu19759=
XM_017004821.1:c.59272G= (TTN) XP_016860310.1:p.Glu19758=
XM_017004822.1:c.56314G= (TTN) XP_016860311.1:p.Glu18772=
XM_017004823.1:c.37930G= (TTN) XP_016860312.1:p.Glu12644=
XM_024453094.1:c.59425G= (TTN) XP_024308862.1:p.Glu19809=
XM_024453095.1:c.59422G= (TTN) XP_024308863.1:p.Glu19808=
XM_024453096.1:c.58855G= (TTN) XP_024308864.1:p.Glu19619=
XM_024453097.1:c.56197G= (TTN) XP_024308865.1:p.Glu18733=
XM_024453098.1:c.56116G= (TTN) XP_024308866.1:p.Glu18706=
XM_024453099.1:c.37879G= (TTN) XP_024308867.1:p.Glu12627=
XM_024453100.1:c.27733G= (TTN) XP_024308868.1:p.Glu9245=