Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.38363190_38363191insT , CM000682.2:g.38363190_38363191insT | GRCh38 |
| NC_000020.10:g.36991844_36991845insT , CM000682.1:g.36991844_36991845insT | GRCh37 |
| NC_000020.9:g.36425258_36425259insT | NCBI36 |
| NG_034239.1:g.21780_21781insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217407.3:c.653-785_653-784insT MANE Select | ENSP00000217407.2:n.653-785_653-784insT | |
| ENST00000217407.2:c.653-785_653-784insT | ENSP00000217407.2:n.653-785_653-784insT | |
| NM_004139.4:c.653-785_653-784insT | NP_004130.2:n.653-785_653-784insT | |
| NM_004139.5:c.653-785_653-784insT MANE Select | NP_004130.2:n.653-785_653-784insT |