Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.25013689_25013692delinsCGCT , CM000685.2:g.25013689_25013692delinsCGCT | GRCh38 |
| NC_000023.10:g.25031806_25031809delinsCGCT , CM000685.1:g.25031806_25031809delinsCGCT | GRCh37 |
| NC_000023.9:g.24941727_24941730delinsCGCT | NCBI36 |
| NG_008281.1:g.7257_7260delinsAGCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000379044.5:c.303_306delinsAGCG MANE Select | ENSP00000368332.4:p.Ala101= | |
| ENST00000379044.4:c.303_306delinsAGCG | ENSP00000368332.4:p.Ala101= | |
| NM_139058.2:c.303_306delinsAGCG | NP_620689.1:p.Ala101= | |
| NM_139058.3:c.303_306delinsAGCG MANE Select | NP_620689.1:p.Ala101= |