Linked Data
gnomAD v4:
X-151181398-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.151181399del , CM000685.2:g.151181399del | GRCh38 |
| NC_000023.10:g.150349871del , CM000685.1:g.150349871del | GRCh37 |
| NC_000023.9:g.150100529del | NCBI36 |
| NG_016405.1:g.9816del | |
| NG_016405.2:g.9816del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218316.4:c.1816del MANE Select | ENSP00000218316.3:p.Ile606LeufsTer? | |
| ENST00000218316.3:c.1816del | ENSP00000218316.3:p.Ile606LeufsTer? | |
| ENST00000617907.1:c.1810del | ENSP00000484496.1:p.Ile604LeufsTer? | |
| NM_004224.3:c.1816del MANE Select | NP_004215.2:p.Ile606LeufsTer? | |
| XM_011531216.1:c.1075del | XP_011529518.1:p.Ile359LeufsTer? | |
| XM_011531216.2:c.1075del | XP_011529518.1:p.Ile359LeufsTer? |