Canonical Allele Identifier: CA1310522195

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178552677G= , CM000664.2:g.178552677G= GRCh38
NC_000002.11:g.179417404G= , CM000664.1:g.179417404G= GRCh37
NC_000002.10:g.179125650G= NCBI36
NG_011618.3:g.283126C= , LRG_391:g.283126C=
NG_051363.1:g.34851G=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.82519C= (TTN) ENSP00000343764.6:p.Gln27507=
ENST00000342175.11:c.63604C= (TTN) ENSP00000340554.6:p.Gln21202=
ENST00000359218.10:c.63403C= (TTN) ENSP00000352154.5:p.Gln21135=
ENST00000342175.10:c.63604C= (TTN) ENSP00000340554.6:p.Gln21202=
ENST00000342992.10:c.82519C= (TTN) ENSP00000343764.6:p.Gln27507=
ENST00000359218.9:c.63403C= (TTN) ENSP00000352154.5:p.Gln21135=
ENST00000460472.6:c.63028C= (TTN) ENSP00000434586.1:p.Gln21010=
ENST00000589042.5:c.90223C= (TTN) MANE Select ENSP00000467141.1:p.Gln30075=
ENST00000591111.5:c.85300C= (TTN) ENSP00000465570.1:p.Gln28434=
ENST00000615779.4:c.85300C= (TTN) ENSP00000483597.1:p.Gln28434=
NM_001256850.1:c.85300C= (TTN) NP_001243779.1:p.Gln28434=
NM_001267550.2:c.90223C= (TTN) MANE Select NP_001254479.2:p.Gln30075=
NM_003319.4:c.63028C= (TTN) NP_003310.4:p.Gln21010=
NM_133378.4:c.82519C= (TTN) NP_596869.4:p.Gln27507=
NM_133432.3:c.63403C= (TTN) NP_597676.3:p.Gln21135=
NM_133437.4:c.63604C= (TTN) NP_597681.4:p.Gln21202=
NR_038271.1:n.447-18623G= (TTN-AS1)
NR_038272.1:n.2043+10316G= (TTN-AS1)
XM_011511729.1:c.89320C= (TTN) XP_011510031.1:p.Gln29774=
XM_011511730.1:c.63214C= (TTN) XP_011510032.1:p.Gln21072=
XM_011511731.1:c.63073C= (TTN) XP_011510033.1:p.Gln21025=
XM_017004819.1:c.89116C= (TTN) XP_016860308.1:p.Gln29706=
XM_017004820.1:c.84514C= (TTN) XP_016860309.1:p.Gln28172=
XM_017004821.1:c.84511C= (TTN) XP_016860310.1:p.Gln28171=
XM_017004822.1:c.81553C= (TTN) XP_016860311.1:p.Gln27185=
XM_017004823.1:c.63169C= (TTN) XP_016860312.1:p.Gln21057=
XM_024453094.1:c.84664C= (TTN) XP_024308862.1:p.Gln28222=
XM_024453095.1:c.84661C= (TTN) XP_024308863.1:p.Gln28221=
XM_024453096.1:c.84094C= (TTN) XP_024308864.1:p.Gln28032=
XM_024453097.1:c.81436C= (TTN) XP_024308865.1:p.Gln27146=
XM_024453098.1:c.81355C= (TTN) XP_024308866.1:p.Gln27119=
XM_024453099.1:c.63118C= (TTN) XP_024308867.1:p.Gln21040=
XM_024453100.1:c.52972C= (TTN) XP_024308868.1:p.Gln17658=