Canonical Allele Identifier: CA2586970739

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178530499_178530500insTT , CM000664.2:g.178530499_178530500insTT GRCh38
NC_000002.11:g.179395226_179395227insTT , CM000664.1:g.179395226_179395227insTT GRCh37
NC_000002.10:g.179103472_179103473insTT NCBI36
NG_011618.3:g.305304_305305insAA , LRG_391:g.305304_305305insAA
NG_051363.1:g.12673_12674insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.98412_98413insAA (TTN) ENSP00000343764.6:p.Gln32805AsnfsTer?
ENST00000342175.11:c.79497_79498insAA (TTN) ENSP00000340554.6:p.Gln26500AsnfsTer?
ENST00000359218.10:c.79296_79297insAA (TTN) ENSP00000352154.5:p.Gln26433AsnfsTer?
ENST00000342175.10:c.79497_79498insAA (TTN) ENSP00000340554.6:p.Gln26500AsnfsTer?
ENST00000342992.10:c.98412_98413insAA (TTN) ENSP00000343764.6:p.Gln32805AsnfsTer?
ENST00000359218.9:c.79296_79297insAA (TTN) ENSP00000352154.5:p.Gln26433AsnfsTer?
ENST00000460472.6:c.78921_78922insAA (TTN) ENSP00000434586.1:p.Gln26308AsnfsTer?
ENST00000589042.5:c.106116_106117insAA (TTN) MANE Select ENSP00000467141.1:p.Gln35373AsnfsTer?
ENST00000591111.5:c.101193_101194insAA (TTN) ENSP00000465570.1:p.Gln33732AsnfsTer?
ENST00000615779.4:c.101193_101194insAA (TTN) ENSP00000483597.1:p.Gln33732AsnfsTer?
NM_001256850.1:c.101193_101194insAA (TTN) NP_001243779.1:p.Gln33732AsnfsTer?
NM_001267550.2:c.106116_106117insAA (TTN) MANE Select NP_001254479.2:p.Gln35373AsnfsTer?
NM_003319.4:c.78921_78922insAA (TTN) NP_003310.4:p.Gln26308AsnfsTer?
NM_133378.4:c.98412_98413insAA (TTN) NP_596869.4:p.Gln32805AsnfsTer?
NM_133432.3:c.79296_79297insAA (TTN) NP_597676.3:p.Gln26433AsnfsTer?
NM_133437.4:c.79497_79498insAA (TTN) NP_597681.4:p.Gln26500AsnfsTer?
NR_038271.1:n.446+6863_446+6864insTT (TTN-AS1)
NR_038272.1:n.220-5233_220-5232insTT (TTN-AS1)
XM_011511729.1:c.105213_105214insAA (TTN) XP_011510031.1:p.Gln35072AsnfsTer?
XM_011511730.1:c.79107_79108insAA (TTN) XP_011510032.1:p.Gln26370AsnfsTer?
XM_011511731.1:c.78966_78967insAA (TTN) XP_011510033.1:p.Gln26323AsnfsTer?
XM_017004819.1:c.105009_105010insAA (TTN) XP_016860308.1:p.Gln35004AsnfsTer?
XM_017004820.1:c.100407_100408insAA (TTN) XP_016860309.1:p.Gln33470AsnfsTer?
XM_017004821.1:c.100404_100405insAA (TTN) XP_016860310.1:p.Gln33469AsnfsTer?
XM_017004822.1:c.97446_97447insAA (TTN) XP_016860311.1:p.Gln32483AsnfsTer?
XM_017004823.1:c.79062_79063insAA (TTN) XP_016860312.1:p.Gln26355AsnfsTer?
XM_024453094.1:c.100557_100558insAA (TTN) XP_024308862.1:p.Gln33520AsnfsTer?
XM_024453095.1:c.100554_100555insAA (TTN) XP_024308863.1:p.Gln33519AsnfsTer?
XM_024453096.1:c.99987_99988insAA (TTN) XP_024308864.1:p.Gln33330AsnfsTer?
XM_024453097.1:c.97329_97330insAA (TTN) XP_024308865.1:p.Gln32444AsnfsTer?
XM_024453098.1:c.97248_97249insAA (TTN) XP_024308866.1:p.Gln32417AsnfsTer?
XM_024453099.1:c.79011_79012insAA (TTN) XP_024308867.1:p.Gln26338AsnfsTer?
XM_024453100.1:c.68865_68866insAA (TTN) XP_024308868.1:p.Gln22956AsnfsTer?