Linked Data
dbSNP Id:
rs756809636
ExAC:
16:1561183 TC / T
gnomAD v2:
16-1561183-TC-T
gnomAD v3:
16-1511182-TC-T
gnomAD v4:
16-1511182-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.1511184del , CM000678.2:g.1511184del | GRCh38 |
| NC_000016.9:g.1561185del , CM000678.1:g.1561185del | GRCh37 |
| NC_000016.8:g.1501186del | NCBI36 |
| NG_032783.1:g.105926del | |
| NG_050910.1:g.22841del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426508.7:c.4183-33del MANE Select | ENSP00000406012.2:n.4183-33del | |
| ENST00000361339.9:c.1765-33del | ENSP00000354895.5:n.1765-33del | |
| ENST00000397417.6:c.*2621-33del | ENSP00000380562.2:n.*2621-33del | |
| ENST00000426508.6:c.4183-33del | ENSP00000406012.2:n.4183-33del | |
| ENST00000565298.5:n.4007-33del | ||
| NM_014714.3:c.4183-33del | NP_055529.2:n.4183-33del | |
| XM_006720989.2:c.4183-33del | XP_006721052.1:n.4183-33del | |
| XM_006720990.2:c.4183-33del | XP_006721053.1:n.4183-33del | |
| XM_006720991.2:c.4183-33del | XP_006721054.1:n.4183-33del | |
| XM_006720992.2:c.1816-33del | XP_006721055.1:n.1816-33del | |
| XM_011522766.1:c.3937-33del | XP_011521068.1:n.3937-33del | |
| XM_011522767.1:c.3208-33del | XP_011521069.1:n.3208-33del | |
| XM_006720990.3:c.4183-33del | XP_006721053.1:n.4183-33del | |
| XM_006720991.3:c.4183-33del | XP_006721054.1:n.4183-33del | |
| XM_006720992.3:c.1816-33del | XP_006721055.1:n.1816-33del | |
| XM_011522766.3:c.3937-33del | XP_011521068.1:n.3937-33del | |
| XM_011522767.2:c.3208-33del | XP_011521069.1:n.3208-33del | |
| XM_017023910.1:c.4183-33del | XP_016879399.1:n.4183-33del | |
| XM_017023911.1:c.2368-33del | XP_016879400.1:n.2368-33del | |
| NM_014714.4:c.4183-33del MANE Select | NP_055529.2:n.4183-33del |