Linked Data
dbSNP Id:
rs1375855951
gnomAD v2:
17-58227466-GCT-G
gnomAD v3:
17-60150105-GCT-G
gnomAD v4:
17-60150105-GCT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.60150107_60150108del , CM000679.2:g.60150107_60150108del | GRCh38 |
| NC_000017.10:g.58227468_58227469del , CM000679.1:g.58227468_58227469del | GRCh37 |
| NC_000017.9:g.55582250_55582251del | NCBI36 |
| NG_012050.1:g.5167_5168del | |
| NG_012050.2:g.5167_5168del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300900.9:c.58+15_58+16del MANE Select | ENSP00000300900.3:n.58+15_58+16del | |
| ENST00000300900.8:c.58+15_58+16del | ENSP00000300900.3:n.58+15_58+16del | |
| ENST00000585705.5:n.151+15_151+16del | ||
| ENST00000586876.1:c.58+15_58+16del | ENSP00000467465.1:n.58+15_58+16del | |
| ENST00000591725.1:c.-301+15_-301+16del | ENSP00000466964.1:n.-301+15_-301+16del | |
| NM_000717.3:c.58+15_58+16del | NP_000708.1:n.58+15_58+16del | |
| XM_005257639.1:c.58+15_58+16del | XP_005257696.1:n.58+15_58+16del | |
| NM_000717.4:c.58+15_58+16del | NP_000708.1:n.58+15_58+16del | |
| NR_137422.1:n.157+15_157+16del | ||
| XM_005257639.3:c.58+15_58+16del | XP_005257696.1:n.58+15_58+16del | |
| XR_001752604.2:n.151+15_151+16del | ||
| XR_001752605.2:n.151+15_151+16del | ||
| XR_001752606.2:n.151+15_151+16del | ||
| XR_001752607.2:n.151+15_151+16del | ||
| XR_001752608.2:n.151+15_151+16del | ||
| XR_001752609.2:n.151+15_151+16del | ||
| XR_001752610.2:n.151+15_151+16del | ||
| NM_000717.5:c.58+15_58+16del MANE Select | NP_000708.1:n.58+15_58+16del | |
| NR_137422.2:n.120+15_120+16del |