Linked Data
gnomAD v4:
10-119651515-TG-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651517del , CM000672.2:g.119651517del | GRCh38 |
| NC_000010.10:g.121411029del , CM000672.1:g.121411029del | GRCh37 |
| NC_000010.9:g.121401019del | NCBI36 |
| NG_016125.1:g.5148del , LRG_742:g.5148del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.-159del MANE Select | ENSP00000358081.4:n.-159del | |
| ENST00000369085.7:c.-159del | ENSP00000358081.3:n.-159del | |
| NM_004281.3:c.-159del , LRG_742t1:c.-159del | NP_004272.2:n.-159del | |
| XM_005270287.1:c.-159del | XP_005270344.1:n.-159del | |
| XM_005270287.2:c.-159del | XP_005270344.1:n.-159del | |
| NM_004281.4:c.-159del MANE Select | NP_004272.2:n.-159del |