Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.23415083_23415085delinsTTC , CM000676.2:g.23415083_23415085delinsTTC | GRCh38 |
| NC_000014.8:g.23884292_23884294delinsTTC , CM000676.1:g.23884292_23884294delinsTTC | GRCh37 |
| NC_000014.7:g.22954132_22954134delinsTTC | NCBI36 |
| NG_007884.1:g.25577_25579delinsGAA , LRG_384:g.25577_25579delinsGAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355349.4:c.5469_5471delinsGAA MANE Select | ENSP00000347507.3:p.Glu1823= | |
| ENST00000355349.3:c.5469_5471delinsGAA | ENSP00000347507.3:p.Glu1823= | |
| NM_000257.3:c.5469_5471delinsGAA | NP_000248.2:p.Glu1823= | |
| XM_017021340.1:c.5469_5471delinsGAA | XP_016876829.1:p.Glu1823= | |
| NM_000257.4:c.5469_5471delinsGAA MANE Select | NP_000248.2:p.Glu1823= |