Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.38363167_38363168delinsCT , CM000682.2:g.38363167_38363168delinsCT | GRCh38 |
| NC_000020.10:g.36991821_36991822delinsCT , CM000682.1:g.36991821_36991822delinsCT | GRCh37 |
| NC_000020.9:g.36425235_36425236delinsCT | NCBI36 |
| NG_034239.1:g.21757_21758delinsCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217407.3:c.653-808_653-807delinsCT MANE Select | ENSP00000217407.2:n.653-808_653-807delinsCT | |
| ENST00000217407.2:c.653-808_653-807delinsCT | ENSP00000217407.2:n.653-808_653-807delinsCT | |
| NM_004139.4:c.653-808_653-807delinsCT | NP_004130.2:n.653-808_653-807delinsCT | |
| NM_004139.5:c.653-808_653-807delinsCT MANE Select | NP_004130.2:n.653-808_653-807delinsCT |