Canonical Allele Identifier: CA1991078

Linked Data

dbSNP Id: rs768755112

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178577923_178577937del , CM000664.2:g.178577923_178577937del GRCh38
NC_000002.11:g.179442650_179442664del , CM000664.1:g.179442650_179442664del GRCh37
NC_000002.10:g.179150896_179150910del NCBI36
NG_011618.3:g.257872_257886del , LRG_391:g.257872_257886del
NG_051363.1:g.60097_60111del

Transcript Alleles

HGVS Amino-acid Change
ENST00000342992.11:c.60824-33_60824-19del (TTN) ENSP00000343764.6:n.60824-33_60824-19del
ENST00000342175.11:c.41909-33_41909-19del (TTN) ENSP00000340554.6:n.41909-33_41909-19del
ENST00000359218.10:c.41708-33_41708-19del (TTN) ENSP00000352154.5:n.41708-33_41708-19del
ENST00000342175.10:c.41909-33_41909-19del (TTN) ENSP00000340554.6:n.41909-33_41909-19del
ENST00000342992.10:c.60824-33_60824-19del (TTN) ENSP00000343764.6:n.60824-33_60824-19del
ENST00000359218.9:c.41708-33_41708-19del (TTN) ENSP00000352154.5:n.41708-33_41708-19del
ENST00000460472.6:c.41333-33_41333-19del (TTN) ENSP00000434586.1:n.41333-33_41333-19del
ENST00000589042.5:c.68528-33_68528-19del (TTN) MANE Select ENSP00000467141.1:n.68528-33_68528-19del
ENST00000591111.5:c.63605-33_63605-19del (TTN) ENSP00000465570.1:n.63605-33_63605-19del
ENST00000615779.4:c.63605-33_63605-19del (TTN) ENSP00000483597.1:n.63605-33_63605-19del
NM_001256850.1:c.63605-33_63605-19del (TTN) NP_001243779.1:n.63605-33_63605-19del
NM_001267550.2:c.68528-33_68528-19del (TTN) MANE Select NP_001254479.2:n.68528-33_68528-19del
NM_003319.4:c.41333-33_41333-19del (TTN) NP_003310.4:n.41333-33_41333-19del
NM_133378.4:c.60824-33_60824-19del (TTN) NP_596869.4:n.60824-33_60824-19del
NM_133432.3:c.41708-33_41708-19del (TTN) NP_597676.3:n.41708-33_41708-19del
NM_133437.4:c.41909-33_41909-19del (TTN) NP_597681.4:n.41909-33_41909-19del
NR_038271.1:n.596+6474_596+6488del (TTN-AS1)
NR_038272.1:n.2044-4649_2044-4635del (TTN-AS1)
XM_011511729.1:c.67625-33_67625-19del (TTN) XP_011510031.1:n.67625-33_67625-19del
XM_011511730.1:c.41519-33_41519-19del (TTN) XP_011510032.1:n.41519-33_41519-19del
XM_011511731.1:c.41378-33_41378-19del (TTN) XP_011510033.1:n.41378-33_41378-19del
XM_017004819.1:c.67421-33_67421-19del (TTN) XP_016860308.1:n.67421-33_67421-19del
XM_017004820.1:c.62819-33_62819-19del (TTN) XP_016860309.1:n.62819-33_62819-19del
XM_017004821.1:c.62816-33_62816-19del (TTN) XP_016860310.1:n.62816-33_62816-19del
XM_017004822.1:c.59858-33_59858-19del (TTN) XP_016860311.1:n.59858-33_59858-19del
XM_017004823.1:c.41474-33_41474-19del (TTN) XP_016860312.1:n.41474-33_41474-19del
XM_024453094.1:c.62969-33_62969-19del (TTN) XP_024308862.1:n.62969-33_62969-19del
XM_024453095.1:c.62966-33_62966-19del (TTN) XP_024308863.1:n.62966-33_62966-19del
XM_024453096.1:c.62399-33_62399-19del (TTN) XP_024308864.1:n.62399-33_62399-19del
XM_024453097.1:c.59741-33_59741-19del (TTN) XP_024308865.1:n.59741-33_59741-19del
XM_024453098.1:c.59660-33_59660-19del (TTN) XP_024308866.1:n.59660-33_59660-19del
XM_024453099.1:c.41423-33_41423-19del (TTN) XP_024308867.1:n.41423-33_41423-19del
XM_024453100.1:c.31277-33_31277-19del (TTN) XP_024308868.1:n.31277-33_31277-19del