Linked Data
gnomAD v4:
4-42963231-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.42963232del , CM000666.2:g.42963232del | GRCh38 |
| NC_000004.11:g.42965249del , CM000666.1:g.42965249del | GRCh37 |
| NC_000004.10:g.42660006del | NCBI36 |
| NG_027718.1:g.74967del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000399770.3:c.627+98del MANE Select | ENSP00000382670.2:n.627+98del | |
| ENST00000399770.2:c.627+98del | ENSP00000382670.2:n.627+98del | |
| NM_001080476.2:c.627+98del | NP_001073945.1:n.627+98del | |
| XM_011513691.1:c.264+98del | XP_011511993.1:n.264+98del | |
| NM_001080476.3:c.627+98del MANE Select | NP_001073945.1:n.627+98del |