Canonical Allele Identifier: CA1310540446

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178593235T= , CM000664.2:g.178593235T= GRCh38
NC_000002.11:g.179457962T= , CM000664.1:g.179457962T= GRCh37
NC_000002.10:g.179166208T= NCBI36
NG_011618.3:g.242568A= , LRG_391:g.242568A=
NG_051363.1:g.75409T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.51269A= (TTN) ENSP00000343764.6:p.Asn17090=
ENST00000342175.11:c.32354A= (TTN) ENSP00000340554.6:p.Asn10785=
ENST00000359218.10:c.32153A= (TTN) ENSP00000352154.5:p.Asn10718=
ENST00000342175.10:c.32354A= (TTN) ENSP00000340554.6:p.Asn10785=
ENST00000342992.10:c.51269A= (TTN) ENSP00000343764.6:p.Asn17090=
ENST00000359218.9:c.32153A= (TTN) ENSP00000352154.5:p.Asn10718=
ENST00000460472.6:c.31778A= (TTN) ENSP00000434586.1:p.Asn10593=
ENST00000589042.5:c.58973A= (TTN) MANE Select ENSP00000467141.1:p.Asn19658=
ENST00000591111.5:c.54050A= (TTN) ENSP00000465570.1:p.Asn18017=
ENST00000615779.4:c.54050A= (TTN) ENSP00000483597.1:p.Asn18017=
NM_001256850.1:c.54050A= (TTN) NP_001243779.1:p.Asn18017=
NM_001267550.2:c.58973A= (TTN) MANE Select NP_001254479.2:p.Asn19658=
NM_003319.4:c.31778A= (TTN) NP_003310.4:p.Asn10593=
NM_133378.4:c.51269A= (TTN) NP_596869.4:p.Asn17090=
NM_133432.3:c.32153A= (TTN) NP_597676.3:p.Asn10718=
NM_133437.4:c.32354A= (TTN) NP_597681.4:p.Asn10785=
NR_038271.1:n.597-4361T= (TTN-AS1)
NR_038272.1:n.3364+1921T= (TTN-AS1)
XM_011511729.1:c.58070A= (TTN) XP_011510031.1:p.Asn19357=
XM_011511730.1:c.31964A= (TTN) XP_011510032.1:p.Asn10655=
XM_011511731.1:c.31823A= (TTN) XP_011510033.1:p.Asn10608=
XM_017004819.1:c.57866A= (TTN) XP_016860308.1:p.Asn19289=
XM_017004820.1:c.53264A= (TTN) XP_016860309.1:p.Asn17755=
XM_017004821.1:c.53261A= (TTN) XP_016860310.1:p.Asn17754=
XM_017004822.1:c.50303A= (TTN) XP_016860311.1:p.Asn16768=
XM_017004823.1:c.31919A= (TTN) XP_016860312.1:p.Asn10640=
XM_024453094.1:c.53414A= (TTN) XP_024308862.1:p.Asn17805=
XM_024453095.1:c.53411A= (TTN) XP_024308863.1:p.Asn17804=
XM_024453096.1:c.52844A= (TTN) XP_024308864.1:p.Asn17615=
XM_024453097.1:c.50186A= (TTN) XP_024308865.1:p.Asn16729=
XM_024453098.1:c.50105A= (TTN) XP_024308866.1:p.Asn16702=
XM_024453099.1:c.31868A= (TTN) XP_024308867.1:p.Asn10623=
XM_024453100.1:c.21722A= (TTN) XP_024308868.1:p.Asn7241=