Linked Data
gnomAD v4:
22-37713387-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.37713388del , CM000684.2:g.37713388del | GRCh38 |
| NC_000022.10:g.38109395del , CM000684.1:g.38109395del | GRCh37 |
| NC_000022.9:g.36439341del | NCBI36 |
| NG_012857.1:g.21401del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644935.1:c.433del MANE Select | ENSP00000496394.1:p.Asp145IlefsTer28 | |
| ENST00000344404.10:c.255-2375del | ENSP00000340312.6:n.255-2375del | |
| ENST00000406386.7:c.433del | ENSP00000384312.3:p.Asp145IlefsTer28 | |
| ENST00000455236.4:c.1390del | ENSP00000477208.1:n.1390del | |
| ENST00000492485.5:n.391-2375del | ||
| NM_001039141.2:c.433del | NP_001034230.1:p.Asp145IlefsTer28 | |
| NM_001039141.3:c.433del MANE Select | NP_001034230.1:p.Asp145IlefsTer28 |