Canonical Allele Identifier:
CA1138937649
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.8707914_8707915insTTTTTTTTTT , CM000686.2:g.8707914_8707915insTTTTTTTTTT | GRCh38 |
| NC_000024.9:g.8575955_8575956insTTTTTTTTTT , CM000686.1:g.8575955_8575956insTTTTTTTTTT | GRCh37 |
| NC_000024.8:g.8635955_8635956insTTTTTTTTTT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000623558.1:c.139+8882_139+8883insTTTTTTTTTT | ENSP00000485446.1:n.139+8882_139+8883insT... | |
| ENST00000624593.1:c.-57+40801_-57+40802insAAAAAAAAAA | ENSP00000485106.1:n.-57+40801_-57+40802in... |