Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.188991429_188991430insT , CM000664.2:g.188991429_188991430insT | GRCh38 |
| NC_000002.11:g.189856155_189856156insT , CM000664.1:g.189856155_189856156insT | GRCh37 |
| NC_000002.10:g.189564400_189564401insT | NCBI36 |
| NG_007404.1:g.22057_22058insT , LRG_3:g.22057_22058insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450867.2:c.853-58_853-57insT | ENSP00000415346.2:n.853-58_853-57insT | |
| ENST00000304636.9:c.853-58_853-57insT MANE Select | ENSP00000304408.4:n.853-58_853-57insT | |
| ENST00000304636.7:c.853-58_853-57insT | ENSP00000304408.3:n.853-58_853-57insT | |
| ENST00000317840.9:c.853-58_853-57insT | ENSP00000315243.6:n.853-58_853-57insT | |
| NM_000090.3:c.853-58_853-57insT , LRG_3t1:c.853-58_853-57insT | NP_000081.1:n.853-58_853-57insT | |
| NM_000090.4:c.853-58_853-57insT MANE Select | NP_000081.2:n.853-58_853-57insT |