Linked Data
dbSNP Id:
rs912697528
gnomAD v2:
16-50756780-TTTCTGGGTGAC-T
gnomAD v3:
16-50722869-TTTCTGGGTGAC-T
gnomAD v4:
16-50722869-TTTCTGGGTGAC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.50722872_50722882del , CM000678.2:g.50722872_50722882del | GRCh38 |
| NC_000016.9:g.50756783_50756793del , CM000678.1:g.50756783_50756793del | GRCh37 |
| NC_000016.8:g.49314284_49314294del | NCBI36 |
| NG_007508.1:g.30734_30744del , LRG_177:g.30734_30744del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000641284.2:c.2382-6946_2382-6936del | ENSP00000493088.1:n.2382-6946_2382-6936de... | |
| ENST00000646677.2:c.*482+167_*482+177del | ENSP00000496533.1:n.*482+167_*482+177del | |
| ENST00000697425.1:c.544+167_544+177del | ||
| ENST00000697426.1:c.432+167_432+177del | ||
| ENST00000697427.1:c.348+167_348+177del | ||
| ENST00000697428.1:n.2195+167_2195+177del | ||
| ENST00000641284.1:c.2382-6946_2382-6936del | ENSP00000493088.1:n.2382-6946_2382-6936de... | |
| ENST00000646677.1:c.*482+167_*482+177del | ENSP00000496533.1:n.*482+167_*482+177del | |
| ENST00000647318.2:c.2717+167_2717+177del MANE Select | ENSP00000495993.1:n.2717+167_2717+177del | |
| ENST00000300589.6:c.2798+167_2798+177del | ENSP00000300589.2:n.2798+167_2798+177del | |
| ENST00000524712.5:c.292+167_292+177del | ||
| ENST00000527052.5:c.264+167_264+177del | ||
| ENST00000529633.5:c.376+167_376+177del | ||
| ENST00000534057.1:c.432+167_432+177del | ||
| ENST00000534067.5:c.528+167_528+177del | ||
| NM_001293557.1:c.2717+167_2717+177del | NP_001280486.1:n.2717+167_2717+177del | |
| NM_022162.2:c.2798+167_2798+177del | NP_071445.1:n.2798+167_2798+177del | |
| XM_005256084.2:c.2717+167_2717+177del | XP_005256141.1:n.2717+167_2717+177del | |
| XM_006721242.2:c.2633+167_2633+177del | XP_006721305.1:n.2633+167_2633+177del | |
| XM_011523257.1:c.2294+167_2294+177del | XP_011521559.1:n.2294+167_2294+177del | |
| XM_011523258.1:c.2294+167_2294+177del | XP_011521560.1:n.2294+167_2294+177del | |
| XM_011523259.1:c.2132+167_2132+177del | XP_011521561.1:n.2132+167_2132+177del | |
| XR_429725.2:n.2639+167_2639+177del | ||
| XR_429726.2:n.2555+167_2555+177del | ||
| XR_933387.1:n.2835+167_2835+177del | ||
| XM_005256084.4:c.2717+167_2717+177del | XP_005256141.1:n.2717+167_2717+177del | |
| XM_006721242.4:c.2633+167_2633+177del | XP_006721305.1:n.2633+167_2633+177del | |
| XM_011523259.2:c.2132+167_2132+177del | XP_011521561.1:n.2132+167_2132+177del | |
| XM_017023535.1:c.2225+167_2225+177del | XP_016879024.1:n.2225+167_2225+177del | |
| XM_017023536.1:c.2132+167_2132+177del | XP_016879025.1:n.2132+167_2132+177del | |
| XM_017023537.1:c.2132+167_2132+177del | XP_016879026.1:n.2132+167_2132+177del | |
| XM_017023538.1:c.2132+167_2132+177del | XP_016879027.1:n.2132+167_2132+177del | |
| XR_429725.3:n.2592+167_2592+177del | ||
| XR_429726.3:n.2508+167_2508+177del | ||
| XR_933387.2:n.2788+167_2788+177del | ||
| NM_001293557.2:c.2717+167_2717+177del | NP_001280486.1:n.2717+167_2717+177del | |
| NM_001370466.1:c.2717+167_2717+177del MANE Select | NP_001357395.1:n.2717+167_2717+177del | |
| NM_022162.3:c.2798+167_2798+177del | NP_071445.1:n.2798+167_2798+177del | |
| NR_163434.1:n.2929+167_2929+177del |