Linked Data
gnomAD v4:
X-154905053-AGC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154905054_154905055del , CM000685.2:g.154905054_154905055del | GRCh38 |
| NC_000023.10:g.154133329_154133330del , CM000685.1:g.154133329_154133330del | GRCh37 |
| NC_000023.9:g.153786523_153786524del | NCBI36 |
| NG_011403.1:g.122669_122670del | |
| NG_011403.2:g.122669_122670del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5374-32_5374-31del MANE Select | ENSP00000353393.4:n.5374-32_5374-31del | |
| ENST00000360256.8:c.5374-32_5374-31del | ENSP00000353393.4:n.5374-32_5374-31del | |
| NM_000132.3:c.5374-32_5374-31del | NP_000123.1:n.5374-32_5374-31del | |
| XM_011531126.1:c.5269-32_5269-31del | XP_011529428.1:n.5269-32_5269-31del | |
| NM_000132.4:c.5374-32_5374-31del MANE Select | NP_000123.1:n.5374-32_5374-31del |