Canonical Allele Identifier: CA273567

Linked Data

ClinVar Variation Id: 178913
dbSNP Id: rs727504535

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178538837del , CM000664.2:g.178538837del GRCh38
NC_000002.11:g.179403564del , CM000664.1:g.179403564del GRCh37
NC_000002.10:g.179111810del NCBI36
NG_011618.3:g.296968del , LRG_391:g.296968del
NG_051363.1:g.21011del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.91290del (TTN) ENSP00000343764.6:p.Lys30430AsnfsTer?
ENST00000342175.11:c.72375del (TTN) ENSP00000340554.6:p.Lys24125AsnfsTer?
ENST00000359218.10:c.72174del (TTN) ENSP00000352154.5:p.Lys24058AsnfsTer?
ENST00000342175.10:c.72375del (TTN) ENSP00000340554.6:p.Lys24125AsnfsTer?
ENST00000342992.10:c.91290del (TTN) ENSP00000343764.6:p.Lys30430AsnfsTer?
ENST00000359218.9:c.72174del (TTN) ENSP00000352154.5:p.Lys24058AsnfsTer?
ENST00000460472.6:c.71799del (TTN) ENSP00000434586.1:p.Lys23933AsnfsTer?
ENST00000589042.5:c.98994del (TTN) MANE Select ENSP00000467141.1:p.Lys32998AsnfsTer?
ENST00000591111.5:c.94071del (TTN) ENSP00000465570.1:p.Lys31357AsnfsTer?
ENST00000615779.4:c.94071del (TTN) ENSP00000483597.1:p.Lys31357AsnfsTer?
NM_001256850.1:c.94071del (TTN) NP_001243779.1:p.Lys31357AsnfsTer?
NM_001267550.2:c.98994del (TTN) MANE Select NP_001254479.2:p.Lys32998AsnfsTer?
NM_003319.4:c.71799del (TTN) NP_003310.4:p.Lys23933AsnfsTer?
NM_133378.4:c.91290del (TTN) NP_596869.4:p.Lys30430AsnfsTer?
NM_133432.3:c.72174del (TTN) NP_597676.3:p.Lys24058AsnfsTer?
NM_133437.4:c.72375del (TTN) NP_597681.4:p.Lys24125AsnfsTer?
NR_038271.1:n.446+15201del (TTN-AS1)
NR_038272.1:n.787del (TTN-AS1)
XM_011511729.1:c.98091del (TTN) XP_011510031.1:p.Lys32697AsnfsTer?
XM_011511730.1:c.71985del (TTN) XP_011510032.1:p.Lys23995AsnfsTer?
XM_011511731.1:c.71844del (TTN) XP_011510033.1:p.Lys23948AsnfsTer?
XM_017004819.1:c.97887del (TTN) XP_016860308.1:p.Lys32629AsnfsTer?
XM_017004820.1:c.93285del (TTN) XP_016860309.1:p.Lys31095AsnfsTer?
XM_017004821.1:c.93282del (TTN) XP_016860310.1:p.Lys31094AsnfsTer?
XM_017004822.1:c.90324del (TTN) XP_016860311.1:p.Lys30108AsnfsTer?
XM_017004823.1:c.71940del (TTN) XP_016860312.1:p.Lys23980AsnfsTer?
XM_024453094.1:c.93435del (TTN) XP_024308862.1:p.Lys31145AsnfsTer?
XM_024453095.1:c.93432del (TTN) XP_024308863.1:p.Lys31144AsnfsTer?
XM_024453096.1:c.92865del (TTN) XP_024308864.1:p.Lys30955AsnfsTer?
XM_024453097.1:c.90207del (TTN) XP_024308865.1:p.Lys30069AsnfsTer?
XM_024453098.1:c.90126del (TTN) XP_024308866.1:p.Lys30042AsnfsTer?
XM_024453099.1:c.71889del (TTN) XP_024308867.1:p.Lys23963AsnfsTer?
XM_024453100.1:c.61743del (TTN) XP_024308868.1:p.Lys20581AsnfsTer?