Linked Data
dbSNP Id:
rs556335113
gnomAD v2:
22-29089846-CA-C
gnomAD v3:
22-28693858-CA-C
gnomAD v4:
22-28693858-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28693869del , CM000684.2:g.28693869del | GRCh38 |
| NC_000022.10:g.29089857del , CM000684.1:g.29089857del | GRCh37 |
| NC_000022.9:g.27419857del | NCBI36 |
| NG_008150.1:g.52976del | |
| NG_008150.2:g.53008del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711048.1:c.*196+173del | ENSP00000518557.1:n.*196+173del | |
| ENST00000402731.6:c.1260+173del | ENSP00000384835.2:n.1260+173del | |
| ENST00000404276.6:c.1461+173del MANE Select | ENSP00000385747.1:n.1461+173del | |
| ENST00000425190.7:c.798+173del | ENSP00000390244.2:n.798+173del | |
| ENST00000464581.6:c.801+173del | ENSP00000483777.2:n.801+173del | |
| ENST00000648295.1:n.1013+173del | ||
| ENST00000649563.1:c.798+173del | ENSP00000496928.1:n.798+173del | |
| ENST00000650281.1:c.1461+173del | ENSP00000497000.1:n.1461+173del | |
| ENST00000328354.10:c.1461+173del | ENSP00000329178.6:n.1461+173del | |
| ENST00000348295.7:c.1374+173del | ENSP00000329012.5:n.1374+173del | |
| ENST00000382580.6:c.1590+173del | ENSP00000372023.2:n.1590+173del | |
| ENST00000402731.5:c.1374+173del | ENSP00000384835.1:n.1374+173del | |
| ENST00000403642.5:c.1188+173del | ENSP00000384919.1:n.1188+173del | |
| ENST00000404276.5:c.1461+173del | ENSP00000385747.1:n.1461+173del | |
| ENST00000405598.5:c.1461+173del | ENSP00000386087.1:n.1461+173del | |
| ENST00000416671.5:c.*951+173del | ENSP00000402225.1:n.*951+173del | |
| ENST00000417588.5:c.1370+173del | ENSP00000412901.1:n.1370+173del | |
| ENST00000433728.5:c.1399+173del | ENSP00000404400.1:n.1399+173del | |
| ENST00000434810.5:c.659+173del | ||
| ENST00000448511.5:c.1351+173del | ENSP00000404567.1:n.1351+173del | |
| ENST00000456369.5:c.264-4644del | ||
| NM_001005735.1:c.1590+173del | NP_001005735.1:n.1590+173del | |
| NM_001257387.1:c.798+173del | NP_001244316.1:n.798+173del | |
| NM_007194.3:c.1461+173del | NP_009125.1:n.1461+173del | |
| NM_145862.2:c.1374+173del | NP_665861.1:n.1374+173del | |
| XM_006724114.2:c.981+173del | XP_006724177.1:n.981+173del | |
| XM_006724116.2:c.918+173del | XP_006724179.2:n.918+173del | |
| XM_011529839.1:c.1620+173del | XP_011528141.1:n.1620+173del | |
| XM_011529840.1:c.1533+173del | XP_011528142.1:n.1533+173del | |
| XM_011529841.1:c.1389+173del | XP_011528143.1:n.1389+173del | |
| XM_011529842.1:c.1290+173del | XP_011528144.1:n.1290+173del | |
| XM_011529843.1:c.1260+173del | XP_011528145.1:n.1260+173del | |
| XM_011529845.1:c.798+173del | XP_011528147.1:n.798+173del | |
| XR_937805.1:n.1620+173del | ||
| NM_001349956.1:c.1260+173del | NP_001336885.1:n.1260+173del | |
| NM_007194.4:c.1461+173del MANE Select | NP_009125.1:n.1461+173del | |
| XM_006724114.3:c.1014+173del | XP_006724177.2:n.1014+173del | |
| XM_011529839.2:c.1620+173del | XP_011528141.1:n.1620+173del | |
| XM_011529840.3:c.1533+173del | XP_011528142.1:n.1533+173del | |
| XM_011529842.2:c.1290+173del | XP_011528144.1:n.1290+173del | |
| XM_011529845.2:c.798+173del | XP_011528147.1:n.798+173del | |
| XM_017028560.1:c.1584+173del | XP_016884049.1:n.1584+173del | |
| XM_017028561.2:c.798+173del | XP_016884050.1:n.798+173del | |
| XM_024452148.1:c.1491+173del | XP_024307916.1:n.1491+173del | |
| XM_024452149.1:c.1404+173del | XP_024307917.1:n.1404+173del | |
| XR_937805.2:n.1631+173del | ||
| NM_001005735.2:c.1590+173del | NP_001005735.1:n.1590+173del | |
| NM_001257387.2:c.798+173del | NP_001244316.1:n.798+173del | |
| NM_001349956.2:c.1260+173del | NP_001336885.1:n.1260+173del |