Canonical Allele Identifier: CA1310550904

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178618079C= , CM000664.2:g.178618079C= GRCh38
NC_000002.11:g.179482806C= , CM000664.1:g.179482806C= GRCh37
NC_000002.10:g.179191051C= NCBI36
NG_011618.3:g.217724G= , LRG_391:g.217724G=
NG_051363.1:g.100253C=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39568G= (TTN) ENSP00000343764.6:p.Val13190=
ENST00000342175.11:c.20653G= (TTN) ENSP00000340554.6:p.Val6885=
ENST00000359218.10:c.20452G= (TTN) ENSP00000352154.5:p.Val6818=
ENST00000342175.10:c.20653G= (TTN) ENSP00000340554.6:p.Val6885=
ENST00000342992.10:c.39568G= (TTN) ENSP00000343764.6:p.Val13190=
ENST00000359218.9:c.20452G= (TTN) ENSP00000352154.5:p.Val6818=
ENST00000460472.6:c.20077G= (TTN) ENSP00000434586.1:p.Val6693=
ENST00000589042.5:c.47272G= (TTN) MANE Select ENSP00000467141.1:p.Val15758=
ENST00000591111.5:c.42349G= (TTN) ENSP00000465570.1:p.Val14117=
ENST00000615779.4:c.42349G= (TTN) ENSP00000483597.1:p.Val14117=
NM_001256850.1:c.42349G= (TTN) NP_001243779.1:p.Val14117=
NM_001267550.2:c.47272G= (TTN) MANE Select NP_001254479.2:p.Val15758=
NM_003319.4:c.20077G= (TTN) NP_003310.4:p.Val6693=
NM_133378.4:c.39568G= (TTN) NP_596869.4:p.Val13190=
NM_133432.3:c.20452G= (TTN) NP_597676.3:p.Val6818=
NM_133437.4:c.20653G= (TTN) NP_597681.4:p.Val6885=
NR_038271.1:n.1605-1674C= (TTN-AS1)
XM_011511729.1:c.46369G= (TTN) XP_011510031.1:p.Val15457=
XM_011511730.1:c.20263G= (TTN) XP_011510032.1:p.Val6755=
XM_011511731.1:c.20122G= (TTN) XP_011510033.1:p.Val6708=
XM_017004819.1:c.46165G= (TTN) XP_016860308.1:p.Val15389=
XM_017004820.1:c.41563G= (TTN) XP_016860309.1:p.Val13855=
XM_017004821.1:c.41560G= (TTN) XP_016860310.1:p.Val13854=
XM_017004822.1:c.38602G= (TTN) XP_016860311.1:p.Val12868=
XM_017004823.1:c.20218G= (TTN) XP_016860312.1:p.Val6740=
XM_024453094.1:c.41713G= (TTN) XP_024308862.1:p.Val13905=
XM_024453095.1:c.41710G= (TTN) XP_024308863.1:p.Val13904=
XM_024453096.1:c.41143G= (TTN) XP_024308864.1:p.Val13715=
XM_024453097.1:c.38485G= (TTN) XP_024308865.1:p.Val12829=
XM_024453098.1:c.38404G= (TTN) XP_024308866.1:p.Val12802=
XM_024453099.1:c.20167G= (TTN) XP_024308867.1:p.Val6723=
XM_024453100.1:c.10021G= (TTN) XP_024308868.1:p.Val3341=