Linked Data
gnomAD v4:
15-38253086-GCC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38253092_38253093del , CM000677.2:g.38253092_38253093del | GRCh38 |
| NC_000015.9:g.38545293_38545294del , CM000677.1:g.38545293_38545294del | GRCh37 |
| NC_000015.8:g.36332585_36332586del | NCBI36 |
| NG_008980.1:g.5242_5243del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-94_-93del MANE Select | ENSP00000299084.4:n.-94_-93del | |
| ENST00000299084.8:c.-94_-93del | ENSP00000299084.4:n.-94_-93del | |
| ENST00000561205.1:n.245_246del | ||
| NM_152594.2:c.-94_-93del | NP_689807.1:n.-94_-93del | |
| XM_005254202.2:c.-94_-93del | XP_005254259.1:n.-94_-93del | |
| XM_005254203.3:c.-141_-140del | XP_005254260.1:n.-141_-140del | |
| XM_005254202.3:c.-94_-93del | XP_005254259.1:n.-94_-93del | |
| XR_001751484.1:n.87+479_87+480del | ||
| NM_152594.3:c.-94_-93del MANE Select | NP_689807.1:n.-94_-93del |