Linked Data
dbSNP Id:
rs1788136345
gnomAD v3:
6-161740320-TCTATATCAA-T
gnomAD v4:
6-161740320-TCTATATCAA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.161740324_161740332del , CM000668.2:g.161740324_161740332del | GRCh38 |
| NC_000006.11:g.162161356_162161364del , CM000668.1:g.162161356_162161364del | GRCh37 |
| NC_000006.10:g.162081346_162081354del | NCBI36 |
| NG_008289.1:g.992474_992482del | |
| NG_008289.2:g.992474_992482del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338468.8:c.749+45443_749+45451del | ENSP00000343589.4:n.749+45443_749+45451del | |
| ENST00000366894.6:c.630+45443_630+45451del | ENSP00000355860.2:n.630+45443_630+45451del | |
| ENST00000366898.6:c.871+45443_871+45451del MANE Select | ENSP00000355865.1:n.871+45443_871+45451del | |
| ENST00000673871.1:c.866+45443_866+45451del | ||
| ENST00000674006.1:n.256+45443_256+45451del | ||
| ENST00000674436.1:n.507+45443_507+45451del | ||
| ENST00000674501.1:n.978+45443_978+45451del | ||
| ENST00000338468.7:c.298+45443_298+45451del | ENSP00000343589.3:n.298+45443_298+45451del | |
| ENST00000366892.5:c.871+45443_871+45451del | ENSP00000355858.1:n.871+45443_871+45451del | |
| ENST00000366894.5:c.298+45443_298+45451del | ENSP00000355860.1:n.298+45443_298+45451del | |
| ENST00000366896.5:c.424+45443_424+45451del | ENSP00000355862.1:n.424+45443_424+45451del | |
| ENST00000366897.5:c.787+45443_787+45451del | ENSP00000355863.1:n.787+45443_787+45451del | |
| ENST00000366898.5:c.871+45443_871+45451del | ENSP00000355865.1:n.871+45443_871+45451del | |
| ENST00000479615.5:c.634+45443_634+45451del | ENSP00000434414.1:n.634+45443_634+45451del | |
| NM_004562.2:c.871+45443_871+45451del | NP_004553.2:n.871+45443_871+45451del | |
| NM_013987.2:c.787+45443_787+45451del | NP_054642.2:n.787+45443_787+45451del | |
| NM_013988.2:c.424+45443_424+45451del | NP_054643.2:n.424+45443_424+45451del | |
| XM_011535863.1:c.868+45443_868+45451del | XP_011534165.1:n.868+45443_868+45451del | |
| XM_011535864.1:c.871+45443_871+45451del | XP_011534166.1:n.871+45443_871+45451del | |
| XM_011535865.1:c.871+45443_871+45451del | XP_011534167.1:n.871+45443_871+45451del | |
| XM_017010908.1:c.985+45443_985+45451del | XP_016866397.1:n.985+45443_985+45451del | |
| XM_017010909.2:c.631+45443_631+45451del | XP_016866398.1:n.631+45443_631+45451del | |
| XM_024446449.1:c.634+45443_634+45451del | XP_024302217.1:n.634+45443_634+45451del | |
| XR_001743443.2:n.977+45443_977+45451del | ||
| NM_004562.3:c.871+45443_871+45451del MANE Select | NP_004553.2:n.871+45443_871+45451del | |
| NM_013987.3:c.787+45443_787+45451del | NP_054642.2:n.787+45443_787+45451del | |
| NM_013988.3:c.424+45443_424+45451del | NP_054643.2:n.424+45443_424+45451del |