Linked Data
gnomAD v4:
X-154904717-CTTA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904720_154904722del , CM000685.2:g.154904720_154904722del | GRCh38 |
| NC_000023.10:g.154132995_154132997del , CM000685.1:g.154132995_154132997del | GRCh37 |
| NC_000023.9:g.153786189_153786191del | NCBI36 |
| NG_011403.1:g.123004_123006del | |
| NG_011403.2:g.123004_123006del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5586+91_5586+93del MANE Select | ENSP00000353393.4:n.5586+91_5586+93del | |
| ENST00000360256.8:c.5586+91_5586+93del | ENSP00000353393.4:n.5586+91_5586+93del | |
| NM_000132.3:c.5586+91_5586+93del | NP_000123.1:n.5586+91_5586+93del | |
| XM_011531126.1:c.5481+91_5481+93del | XP_011529428.1:n.5481+91_5481+93del | |
| NM_000132.4:c.5586+91_5586+93del MANE Select | NP_000123.1:n.5586+91_5586+93del |