Linked Data
gnomAD v4:
10-119651453-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651456del , CM000672.2:g.119651456del | GRCh38 |
| NC_000010.10:g.121410968del , CM000672.1:g.121410968del | GRCh37 |
| NC_000010.9:g.121400958del | NCBI36 |
| NG_016125.1:g.5087del , LRG_742:g.5087del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.-220del MANE Select | ENSP00000358081.4:n.-220del | |
| ENST00000369085.7:c.-220del | ENSP00000358081.3:n.-220del | |
| NM_004281.3:c.-220del , LRG_742t1:c.-220del | NP_004272.2:n.-220del | |
| XM_005270287.1:c.-220del | XP_005270344.1:n.-220del | |
| XM_005270287.2:c.-220del | XP_005270344.1:n.-220del | |
| NM_004281.4:c.-220del MANE Select | NP_004272.2:n.-220del |