Linked Data
gnomAD v4:
5-151100826-TCCAAC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151100827_151100831del , CM000667.2:g.151100827_151100831del | GRCh38 |
| NC_000005.9:g.150480388_150480392del , CM000667.1:g.150480388_150480392del | GRCh37 |
| NC_000005.8:g.150460581_150460585del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354546.10:c.*617_*621del MANE Select | ENSP00000346550.5:n.*617_*621del | |
| ENST00000522664.5:c.332_336del | ||
| NM_001155.4:c.*617_*621del | NP_001146.2:n.*617_*621del | |
| NM_001193544.1:c.*617_*621del | NP_001180473.1:n.*617_*621del | |
| NM_001363114.1:c.*617_*621del | NP_001350043.1:n.*617_*621del | |
| NM_001155.5:c.*617_*621del MANE Select | NP_001146.2:n.*617_*621del | |
| NM_001193544.2:c.*617_*621del | NP_001180473.1:n.*617_*621del | |
| NM_001363114.2:c.*617_*621del | NP_001350043.1:n.*617_*621del |