Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23422413_23422414delinsCT , CM000676.2:g.23422413_23422414delinsCT | GRCh38 |
| NC_000014.8:g.23891622_23891623delinsCT , CM000676.1:g.23891622_23891623delinsCT | GRCh37 |
| NC_000014.7:g.22961462_22961463delinsCT | NCBI36 |
| NG_007884.1:g.18248_18249delinsAG , LRG_384:g.18248_18249delinsAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.3100-89_3100-88delinsAG MANE Select | ENSP00000347507.3:n.3100-89_3100-88delinsAG | |
| ENST00000355349.3:c.3100-89_3100-88delinsAG | ENSP00000347507.3:n.3100-89_3100-88delinsAG | |
| NM_000257.3:c.3100-89_3100-88delinsAG | NP_000248.2:n.3100-89_3100-88delinsAG | |
| XR_245686.3:n.3206-89_3206-88delinsAG | ||
| XM_017021340.1:c.3100-89_3100-88delinsAG | XP_016876829.1:n.3100-89_3100-88delinsAG | |
| NM_000257.4:c.3100-89_3100-88delinsAG MANE Select | NP_000248.2:n.3100-89_3100-88delinsAG |