Linked Data
ClinVar Variation Id:
2953335
ClinVar RCV Id:
RCV003810453
dbSNP Id:
rs2092907246
gnomAD v3:
17-42536670-CT-C
gnomAD v4:
17-42536670-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536672del , CM000679.2:g.42536672del | GRCh38 |
| NC_000017.10:g.40688690del , CM000679.1:g.40688690del | GRCh37 |
| NC_000017.9:g.37942216del | NCBI36 |
| NG_011552.1:g.5740del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.383+17del MANE Select | ENSP00000225927.1:n.383+17del | |
| ENST00000225927.6:c.383+17del | ENSP00000225927.1:n.383+17del | |
| ENST00000586516.5:c.133+17del | ||
| ENST00000591587.1:c.126+17del | ENSP00000467836.1:n.126+17del | |
| NM_000263.3:c.383+17del | NP_000254.2:n.383+17del | |
| XM_006721920.2:c.-360+17del | XP_006721983.1:n.-360+17del | |
| XM_011524840.1:c.-360+17del | XP_011523142.1:n.-360+17del | |
| XM_024450771.1:c.383+17del | XP_024306539.1:n.383+17del | |
| NM_000263.4:c.383+17del MANE Select | NP_000254.2:n.383+17del |