Canonical Allele Identifier: CA1310528363

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178564613T= , CM000664.2:g.178564613T= GRCh38
NC_000002.11:g.179429340T= , CM000664.1:g.179429340T= GRCh37
NC_000002.10:g.179137586T= NCBI36
NG_011618.3:g.271190A= , LRG_391:g.271190A=
NG_051363.1:g.46787T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.73815A= (TTN) ENSP00000343764.6:p.Pro24605=
ENST00000342175.11:c.54900A= (TTN) ENSP00000340554.6:p.Pro18300=
ENST00000359218.10:c.54699A= (TTN) ENSP00000352154.5:p.Pro18233=
ENST00000342175.10:c.54900A= (TTN) ENSP00000340554.6:p.Pro18300=
ENST00000342992.10:c.73815A= (TTN) ENSP00000343764.6:p.Pro24605=
ENST00000359218.9:c.54699A= (TTN) ENSP00000352154.5:p.Pro18233=
ENST00000460472.6:c.54324A= (TTN) ENSP00000434586.1:p.Pro18108=
ENST00000589042.5:c.81519A= (TTN) MANE Select ENSP00000467141.1:p.Pro27173=
ENST00000591111.5:c.76596A= (TTN) ENSP00000465570.1:p.Pro25532=
ENST00000615779.4:c.76596A= (TTN) ENSP00000483597.1:p.Pro25532=
NM_001256850.1:c.76596A= (TTN) NP_001243779.1:p.Pro25532=
NM_001267550.2:c.81519A= (TTN) MANE Select NP_001254479.2:p.Pro27173=
NM_003319.4:c.54324A= (TTN) NP_003310.4:p.Pro18108=
NM_133378.4:c.73815A= (TTN) NP_596869.4:p.Pro24605=
NM_133432.3:c.54699A= (TTN) NP_597676.3:p.Pro18233=
NM_133437.4:c.54900A= (TTN) NP_597681.4:p.Pro18300=
NR_038271.1:n.447-6687T= (TTN-AS1)
NR_038272.1:n.2044-17959T= (TTN-AS1)
XM_011511729.1:c.80616A= (TTN) XP_011510031.1:p.Pro26872=
XM_011511730.1:c.54510A= (TTN) XP_011510032.1:p.Pro18170=
XM_011511731.1:c.54369A= (TTN) XP_011510033.1:p.Pro18123=
XM_017004819.1:c.80412A= (TTN) XP_016860308.1:p.Pro26804=
XM_017004820.1:c.75810A= (TTN) XP_016860309.1:p.Pro25270=
XM_017004821.1:c.75807A= (TTN) XP_016860310.1:p.Pro25269=
XM_017004822.1:c.72849A= (TTN) XP_016860311.1:p.Pro24283=
XM_017004823.1:c.54465A= (TTN) XP_016860312.1:p.Pro18155=
XM_024453094.1:c.75960A= (TTN) XP_024308862.1:p.Pro25320=
XM_024453095.1:c.75957A= (TTN) XP_024308863.1:p.Pro25319=
XM_024453096.1:c.75390A= (TTN) XP_024308864.1:p.Pro25130=
XM_024453097.1:c.72732A= (TTN) XP_024308865.1:p.Pro24244=
XM_024453098.1:c.72651A= (TTN) XP_024308866.1:p.Pro24217=
XM_024453099.1:c.54414A= (TTN) XP_024308867.1:p.Pro18138=
XM_024453100.1:c.44268A= (TTN) XP_024308868.1:p.Pro14756=