Canonical Allele Identifier: CA1310515499

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178537535T= , CM000664.2:g.178537535T= GRCh38
NC_000002.11:g.179402262T= , CM000664.1:g.179402262T= GRCh37
NC_000002.10:g.179110508T= NCBI36
NG_011618.3:g.298268A= , LRG_391:g.298268A=
NG_051363.1:g.19709T=

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.91968A= (TTN) ENSP00000343764.6:p.Pro30656=
ENST00000342175.11:c.73053A= (TTN) ENSP00000340554.6:p.Pro24351=
ENST00000359218.10:c.72852A= (TTN) ENSP00000352154.5:p.Pro24284=
ENST00000342175.10:c.73053A= (TTN) ENSP00000340554.6:p.Pro24351=
ENST00000342992.10:c.91968A= (TTN) ENSP00000343764.6:p.Pro30656=
ENST00000359218.9:c.72852A= (TTN) ENSP00000352154.5:p.Pro24284=
ENST00000460472.6:c.72477A= (TTN) ENSP00000434586.1:p.Pro24159=
ENST00000589042.5:c.99672A= (TTN) MANE Select ENSP00000467141.1:p.Pro33224=
ENST00000591111.5:c.94749A= (TTN) ENSP00000465570.1:p.Pro31583=
ENST00000615779.4:c.94749A= (TTN) ENSP00000483597.1:p.Pro31583=
NM_001256850.1:c.94749A= (TTN) NP_001243779.1:p.Pro31583=
NM_001267550.2:c.99672A= (TTN) MANE Select NP_001254479.2:p.Pro33224=
NM_003319.4:c.72477A= (TTN) NP_003310.4:p.Pro24159=
NM_133378.4:c.91968A= (TTN) NP_596869.4:p.Pro30656=
NM_133432.3:c.72852A= (TTN) NP_597676.3:p.Pro24284=
NM_133437.4:c.73053A= (TTN) NP_597681.4:p.Pro24351=
NR_038271.1:n.446+13899T= (TTN-AS1)
NR_038272.1:n.491T= (TTN-AS1)
XM_011511729.1:c.98769A= (TTN) XP_011510031.1:p.Pro32923=
XM_011511730.1:c.72663A= (TTN) XP_011510032.1:p.Pro24221=
XM_011511731.1:c.72522A= (TTN) XP_011510033.1:p.Pro24174=
XM_017004819.1:c.98565A= (TTN) XP_016860308.1:p.Pro32855=
XM_017004820.1:c.93963A= (TTN) XP_016860309.1:p.Pro31321=
XM_017004821.1:c.93960A= (TTN) XP_016860310.1:p.Pro31320=
XM_017004822.1:c.91002A= (TTN) XP_016860311.1:p.Pro30334=
XM_017004823.1:c.72618A= (TTN) XP_016860312.1:p.Pro24206=
XM_024453094.1:c.94113A= (TTN) XP_024308862.1:p.Pro31371=
XM_024453095.1:c.94110A= (TTN) XP_024308863.1:p.Pro31370=
XM_024453096.1:c.93543A= (TTN) XP_024308864.1:p.Pro31181=
XM_024453097.1:c.90885A= (TTN) XP_024308865.1:p.Pro30295=
XM_024453098.1:c.90804A= (TTN) XP_024308866.1:p.Pro30268=
XM_024453099.1:c.72567A= (TTN) XP_024308867.1:p.Pro24189=
XM_024453100.1:c.62421A= (TTN) XP_024308868.1:p.Pro20807=