Canonical Allele Identifier: CA1310526704

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178559631G= , CM000664.2:g.178559631G= GRCh38
NC_000002.11:g.179424358G= , CM000664.1:g.179424358G= GRCh37
NC_000002.10:g.179132604G= NCBI36
NG_011618.3:g.276172C= , LRG_391:g.276172C=
NG_051363.1:g.41805G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.78797C= (TTN) ENSP00000343764.6:p.Ala26266=
ENST00000342175.11:c.59882C= (TTN) ENSP00000340554.6:p.Ala19961=
ENST00000359218.10:c.59681C= (TTN) ENSP00000352154.5:p.Ala19894=
ENST00000342175.10:c.59882C= (TTN) ENSP00000340554.6:p.Ala19961=
ENST00000342992.10:c.78797C= (TTN) ENSP00000343764.6:p.Ala26266=
ENST00000359218.9:c.59681C= (TTN) ENSP00000352154.5:p.Ala19894=
ENST00000460472.6:c.59306C= (TTN) ENSP00000434586.1:p.Ala19769=
ENST00000589042.5:c.86501C= (TTN) MANE Select ENSP00000467141.1:p.Ala28834=
ENST00000591111.5:c.81578C= (TTN) ENSP00000465570.1:p.Ala27193=
ENST00000615779.4:c.81578C= (TTN) ENSP00000483597.1:p.Ala27193=
NM_001256850.1:c.81578C= (TTN) NP_001243779.1:p.Ala27193=
NM_001267550.2:c.86501C= (TTN) MANE Select NP_001254479.2:p.Ala28834=
NM_003319.4:c.59306C= (TTN) NP_003310.4:p.Ala19769=
NM_133378.4:c.78797C= (TTN) NP_596869.4:p.Ala26266=
NM_133432.3:c.59681C= (TTN) NP_597676.3:p.Ala19894=
NM_133437.4:c.59882C= (TTN) NP_597681.4:p.Ala19961=
NR_038271.1:n.447-11669G= (TTN-AS1)
NR_038272.1:n.2043+17270G= (TTN-AS1)
XM_011511729.1:c.85598C= (TTN) XP_011510031.1:p.Ala28533=
XM_011511730.1:c.59492C= (TTN) XP_011510032.1:p.Ala19831=
XM_011511731.1:c.59351C= (TTN) XP_011510033.1:p.Ala19784=
XM_017004819.1:c.85394C= (TTN) XP_016860308.1:p.Ala28465=
XM_017004820.1:c.80792C= (TTN) XP_016860309.1:p.Ala26931=
XM_017004821.1:c.80789C= (TTN) XP_016860310.1:p.Ala26930=
XM_017004822.1:c.77831C= (TTN) XP_016860311.1:p.Ala25944=
XM_017004823.1:c.59447C= (TTN) XP_016860312.1:p.Ala19816=
XM_024453094.1:c.80942C= (TTN) XP_024308862.1:p.Ala26981=
XM_024453095.1:c.80939C= (TTN) XP_024308863.1:p.Ala26980=
XM_024453096.1:c.80372C= (TTN) XP_024308864.1:p.Ala26791=
XM_024453097.1:c.77714C= (TTN) XP_024308865.1:p.Ala25905=
XM_024453098.1:c.77633C= (TTN) XP_024308866.1:p.Ala25878=
XM_024453099.1:c.59396C= (TTN) XP_024308867.1:p.Ala19799=
XM_024453100.1:c.49250C= (TTN) XP_024308868.1:p.Ala16417=