Canonical Allele Identifier: CA1310514307

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178527113T= , CM000664.2:g.178527113T= GRCh38
NC_000002.11:g.179391840T= , CM000664.1:g.179391840T= GRCh37
NC_000002.10:g.179100086T= NCBI36
NG_011618.3:g.308690A= , LRG_391:g.308690A=
NG_051363.1:g.9287T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.100171A= (TTN) ENSP00000343764.6:p.Met33391=
ENST00000342175.11:c.81256A= (TTN) ENSP00000340554.6:p.Met27086=
ENST00000359218.10:c.81055A= (TTN) ENSP00000352154.5:p.Met27019=
ENST00000342175.10:c.81256A= (TTN) ENSP00000340554.6:p.Met27086=
ENST00000342992.10:c.100171A= (TTN) ENSP00000343764.6:p.Met33391=
ENST00000359218.9:c.81055A= (TTN) ENSP00000352154.5:p.Met27019=
ENST00000460472.6:c.80680A= (TTN) ENSP00000434586.1:p.Met26894=
ENST00000589042.5:c.107875A= (TTN) MANE Select ENSP00000467141.1:p.Met35959=
ENST00000591111.5:c.102952A= (TTN) ENSP00000465570.1:p.Met34318=
ENST00000615779.4:c.102952A= (TTN) ENSP00000483597.1:p.Met34318=
NM_001256850.1:c.102952A= (TTN) NP_001243779.1:p.Met34318=
NM_001267550.2:c.107875A= (TTN) MANE Select NP_001254479.2:p.Met35959=
NM_003319.4:c.80680A= (TTN) NP_003310.4:p.Met26894=
NM_133378.4:c.100171A= (TTN) NP_596869.4:p.Met33391=
NM_133432.3:c.81055A= (TTN) NP_597676.3:p.Met27019=
NM_133437.4:c.81256A= (TTN) NP_597681.4:p.Met27086=
NR_038271.1:n.446+3477T= (TTN-AS1)
NR_038272.1:n.219+3477T= (TTN-AS1)
XM_011511729.1:c.106972A= (TTN) XP_011510031.1:p.Met35658=
XM_011511730.1:c.80866A= (TTN) XP_011510032.1:p.Met26956=
XM_011511731.1:c.80725A= (TTN) XP_011510033.1:p.Met26909=
XM_017004819.1:c.106768A= (TTN) XP_016860308.1:p.Met35590=
XM_017004820.1:c.102166A= (TTN) XP_016860309.1:p.Met34056=
XM_017004821.1:c.102163A= (TTN) XP_016860310.1:p.Met34055=
XM_017004822.1:c.99205A= (TTN) XP_016860311.1:p.Met33069=
XM_017004823.1:c.80821A= (TTN) XP_016860312.1:p.Met26941=
XM_024453094.1:c.102316A= (TTN) XP_024308862.1:p.Met34106=
XM_024453095.1:c.102313A= (TTN) XP_024308863.1:p.Met34105=
XM_024453096.1:c.101746A= (TTN) XP_024308864.1:p.Met33916=
XM_024453097.1:c.99088A= (TTN) XP_024308865.1:p.Met33030=
XM_024453098.1:c.99007A= (TTN) XP_024308866.1:p.Met33003=
XM_024453099.1:c.80770A= (TTN) XP_024308867.1:p.Met26924=
XM_024453100.1:c.70624A= (TTN) XP_024308868.1:p.Met23542=