Linked Data
gnomAD v4:
22-32475036-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32475038del , CM000684.2:g.32475038del | GRCh38 |
| NC_000022.10:g.32871025del , CM000684.1:g.32871025del | GRCh37 |
| NC_000022.9:g.31201025del | NCBI36 |
| NG_016001.1:g.5319del | |
| NG_016001.2:g.5319del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.36del MANE Select | ENSP00000266087.7:p.Trp12CysfsTer19 | |
| ENST00000266087.11:c.36del | ENSP00000266087.7:p.Trp12CysfsTer19 | |
| ENST00000420700.5:c.36del | ENSP00000406155.1:p.Trp12CysfsTer19 | |
| ENST00000425028.5:c.36del | ENSP00000395823.1:p.Trp12CysfsTer19 | |
| ENST00000492535.1:n.24del | ||
| NM_012179.3:c.36del | NP_036311.3:p.Trp12CysfsTer19 | |
| XM_011530106.1:c.-138del | XP_011528408.1:n.-138del | |
| XM_024452207.1:c.-155del | XP_024307975.1:n.-155del | |
| NM_012179.4:c.36del MANE Select | NP_036311.3:p.Trp12CysfsTer19 |