Canonical Allele Identifier: CA16610441

Linked Data

dbSNP Id: rs1060500489

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178617513_178617514del , CM000664.2:g.178617513_178617514del GRCh38
NC_000002.11:g.179482240_179482241del , CM000664.1:g.179482240_179482241del GRCh37
NC_000002.10:g.179190485_179190486del NCBI36
NG_011618.3:g.218294_218295del , LRG_391:g.218294_218295del
NG_051363.1:g.99687_99688del

Transcript Alleles

HGVS Amino-acid change
ENST00000342992.11:c.39872_39873del (TTN)
ENST00000342175.11:c.20957_20958del (TTN)
ENST00000359218.10:c.20756_20757del (TTN)
ENST00000342175.10:c.20957_20958del (TTN)
ENST00000342992.10:c.39872_39873del (TTN)
ENST00000359218.9:c.20756_20757del (TTN)
ENST00000460472.6:c.20381_20382del (TTN)
ENST00000589042.5:c.47576_47577del (TTN)
ENST00000591111.5:c.42653_42654del (TTN)
ENST00000615779.4:c.42653_42654del (TTN)
NM_001256850.1:c.42653_42654del (TTN)
NM_001267550.2:c.47576_47577del (TTN)
NM_003319.4:c.20381_20382del (TTN)
NM_133378.4:c.39872_39873del (TTN)
NM_133432.3:c.20756_20757del (TTN)
NM_133437.4:c.20957_20958del (TTN)
NR_038271.1:n.1604+2139_1604+2140del (TTN-AS1)
XM_011511729.1:c.46673_46674del (TTN)
XM_011511730.1:c.20567_20568del (TTN)
XM_011511731.1:c.20426_20427del (TTN)
XM_017004819.1:c.46469_46470del (TTN)
XM_017004820.1:c.41867_41868del (TTN)
XM_017004821.1:c.41864_41865del (TTN)
XM_017004822.1:c.38906_38907del (TTN)
XM_017004823.1:c.20522_20523del (TTN)
XM_024453094.1:c.42017_42018del (TTN)
XM_024453095.1:c.42014_42015del (TTN)
XM_024453096.1:c.41447_41448del (TTN)
XM_024453097.1:c.38789_38790del (TTN)
XM_024453098.1:c.38708_38709del (TTN)
XM_024453099.1:c.20471_20472del (TTN)
XM_024453100.1:c.10325_10326del (TTN)