Canonical Allele Identifier: CA1310514282

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527062C= , CM000664.2:g.178527062C= GRCh38
NC_000002.11:g.179391789C= , CM000664.1:g.179391789C= GRCh37
NC_000002.10:g.179100035C= NCBI36
NG_011618.3:g.308741G= , LRG_391:g.308741G=
NG_051363.1:g.9236C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.100222G= (TTN) ENSP00000343764.6:p.Glu33408=
ENST00000342175.11:c.81307G= (TTN) ENSP00000340554.6:p.Glu27103=
ENST00000359218.10:c.81106G= (TTN) ENSP00000352154.5:p.Glu27036=
ENST00000342175.10:c.81307G= (TTN) ENSP00000340554.6:p.Glu27103=
ENST00000342992.10:c.100222G= (TTN) ENSP00000343764.6:p.Glu33408=
ENST00000359218.9:c.81106G= (TTN) ENSP00000352154.5:p.Glu27036=
ENST00000460472.6:c.80731G= (TTN) ENSP00000434586.1:p.Glu26911=
ENST00000589042.5:c.107926G= (TTN) MANE Select ENSP00000467141.1:p.Glu35976=
ENST00000591111.5:c.103003G= (TTN) ENSP00000465570.1:p.Glu34335=
ENST00000615779.4:c.103003G= (TTN) ENSP00000483597.1:p.Glu34335=
NM_001256850.1:c.103003G= (TTN) NP_001243779.1:p.Glu34335=
NM_001267550.2:c.107926G= (TTN) MANE Select NP_001254479.2:p.Glu35976=
NM_003319.4:c.80731G= (TTN) NP_003310.4:p.Glu26911=
NM_133378.4:c.100222G= (TTN) NP_596869.4:p.Glu33408=
NM_133432.3:c.81106G= (TTN) NP_597676.3:p.Glu27036=
NM_133437.4:c.81307G= (TTN) NP_597681.4:p.Glu27103=
NR_038271.1:n.446+3426C= (TTN-AS1)
NR_038272.1:n.219+3426C= (TTN-AS1)
XM_011511729.1:c.107023G= (TTN) XP_011510031.1:p.Glu35675=
XM_011511730.1:c.80917G= (TTN) XP_011510032.1:p.Glu26973=
XM_011511731.1:c.80776G= (TTN) XP_011510033.1:p.Glu26926=
XM_017004819.1:c.106819G= (TTN) XP_016860308.1:p.Glu35607=
XM_017004820.1:c.102217G= (TTN) XP_016860309.1:p.Glu34073=
XM_017004821.1:c.102214G= (TTN) XP_016860310.1:p.Glu34072=
XM_017004822.1:c.99256G= (TTN) XP_016860311.1:p.Glu33086=
XM_017004823.1:c.80872G= (TTN) XP_016860312.1:p.Glu26958=
XM_024453094.1:c.102367G= (TTN) XP_024308862.1:p.Glu34123=
XM_024453095.1:c.102364G= (TTN) XP_024308863.1:p.Glu34122=
XM_024453096.1:c.101797G= (TTN) XP_024308864.1:p.Glu33933=
XM_024453097.1:c.99139G= (TTN) XP_024308865.1:p.Glu33047=
XM_024453098.1:c.99058G= (TTN) XP_024308866.1:p.Glu33020=
XM_024453099.1:c.80821G= (TTN) XP_024308867.1:p.Glu26941=
XM_024453100.1:c.70675G= (TTN) XP_024308868.1:p.Glu23559=