Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10658450_10658452delinsGCA , CM000682.2:g.10658450_10658452delinsGCA | GRCh38 |
| NC_000020.10:g.10639098_10639100delinsGCA , CM000682.1:g.10639098_10639100delinsGCA | GRCh37 |
| NC_000020.9:g.10587098_10587100delinsGCA | NCBI36 |
| NG_007496.1:g.20595_20597delinsTGC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000254958.10:c.694+16_694+18delinsTGC MANE Select | ENSP00000254958.4:n.694+16_694+18delinsTGC | |
| ENST00000254958.9:c.694+16_694+18delinsTGC | ENSP00000254958.4:n.694+16_694+18delinsTGC | |
| ENST00000423891.6:n.560+16_560+18delinsTGC | ||
| NM_000214.2:c.694+16_694+18delinsTGC | NP_000205.1:n.694+16_694+18delinsTGC | |
| NM_000214.3:c.694+16_694+18delinsTGC MANE Select | NP_000205.1:n.694+16_694+18delinsTGC |