Canonical Allele Identifier: CA1310539766

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178591028T= , CM000664.2:g.178591028T= GRCh38
NC_000002.11:g.179455755T= , CM000664.1:g.179455755T= GRCh37
NC_000002.10:g.179164001T= NCBI36
NG_011618.3:g.244775A= , LRG_391:g.244775A=
NG_051363.1:g.73202T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.52993A= (TTN) ENSP00000343764.6:p.Ile17665=
ENST00000342175.11:c.34078A= (TTN) ENSP00000340554.6:p.Ile11360=
ENST00000359218.10:c.33877A= (TTN) ENSP00000352154.5:p.Ile11293=
ENST00000342175.10:c.34078A= (TTN) ENSP00000340554.6:p.Ile11360=
ENST00000342992.10:c.52993A= (TTN) ENSP00000343764.6:p.Ile17665=
ENST00000359218.9:c.33877A= (TTN) ENSP00000352154.5:p.Ile11293=
ENST00000460472.6:c.33502A= (TTN) ENSP00000434586.1:p.Ile11168=
ENST00000589042.5:c.60697A= (TTN) MANE Select ENSP00000467141.1:p.Ile20233=
ENST00000591111.5:c.55774A= (TTN) ENSP00000465570.1:p.Ile18592=
ENST00000615779.4:c.55774A= (TTN) ENSP00000483597.1:p.Ile18592=
NM_001256850.1:c.55774A= (TTN) NP_001243779.1:p.Ile18592=
NM_001267550.2:c.60697A= (TTN) MANE Select NP_001254479.2:p.Ile20233=
NM_003319.4:c.33502A= (TTN) NP_003310.4:p.Ile11168=
NM_133378.4:c.52993A= (TTN) NP_596869.4:p.Ile17665=
NM_133432.3:c.33877A= (TTN) NP_597676.3:p.Ile11293=
NM_133437.4:c.34078A= (TTN) NP_597681.4:p.Ile11360=
NR_038271.1:n.597-6568T= (TTN-AS1)
NR_038272.1:n.3189-111T= (TTN-AS1)
XM_011511729.1:c.59794A= (TTN) XP_011510031.1:p.Ile19932=
XM_011511730.1:c.33688A= (TTN) XP_011510032.1:p.Ile11230=
XM_011511731.1:c.33547A= (TTN) XP_011510033.1:p.Ile11183=
XM_017004819.1:c.59590A= (TTN) XP_016860308.1:p.Ile19864=
XM_017004820.1:c.54988A= (TTN) XP_016860309.1:p.Ile18330=
XM_017004821.1:c.54985A= (TTN) XP_016860310.1:p.Ile18329=
XM_017004822.1:c.52027A= (TTN) XP_016860311.1:p.Ile17343=
XM_017004823.1:c.33643A= (TTN) XP_016860312.1:p.Ile11215=
XM_024453094.1:c.55138A= (TTN) XP_024308862.1:p.Ile18380=
XM_024453095.1:c.55135A= (TTN) XP_024308863.1:p.Ile18379=
XM_024453096.1:c.54568A= (TTN) XP_024308864.1:p.Ile18190=
XM_024453097.1:c.51910A= (TTN) XP_024308865.1:p.Ile17304=
XM_024453098.1:c.51829A= (TTN) XP_024308866.1:p.Ile17277=
XM_024453099.1:c.33592A= (TTN) XP_024308867.1:p.Ile11198=
XM_024453100.1:c.23446A= (TTN) XP_024308868.1:p.Ile7816=