Linked Data
gnomAD v4:
22-32474938-TCGGCCCCGCCGC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.32474941_32474952del , CM000684.2:g.32474941_32474952del | GRCh38 |
| NC_000022.10:g.32870928_32870939del , CM000684.1:g.32870928_32870939del | GRCh37 |
| NC_000022.9:g.31200928_31200939del | NCBI36 |
| NG_016001.1:g.5222_5233del | |
| NG_016001.2:g.5222_5233del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000266087.12:c.-62_-51del MANE Select | ENSP00000266087.7:n.-62_-51del | |
| ENST00000266087.11:c.-62_-51del | ENSP00000266087.7:n.-62_-51del | |
| ENST00000420700.5:c.-62_-51del | ENSP00000406155.1:n.-62_-51del | |
| ENST00000425028.5:c.-62_-51del | ENSP00000395823.1:n.-62_-51del | |
| NM_012179.3:c.-62_-51del | NP_036311.3:n.-62_-51del | |
| XM_011530106.1:c.-235_-224del | XP_011528408.1:n.-235_-224del | |
| XM_024452207.1:c.-252_-241del | XP_024307975.1:n.-252_-241del | |
| NM_012179.4:c.-62_-51del MANE Select | NP_036311.3:n.-62_-51del |