Linked Data
dbSNP Id:
rs1328055871
gnomAD v2:
20-13782407-GTA-G
gnomAD v3:
20-13801761-GTA-G
gnomAD v4:
20-13801761-GTA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.13801763_13801764del , CM000682.2:g.13801763_13801764del | GRCh38 |
| NC_000020.10:g.13782409_13782410del , CM000682.1:g.13782409_13782410del | GRCh37 |
| NC_000020.9:g.13730409_13730410del | NCBI36 |
| NG_015811.1:g.21738_21739del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378106.10:c.717+80_717+81del MANE Select | ENSP00000367346.5:n.717+80_717+81del | |
| ENST00000378081.9:c.717+80_717+81del | ENSP00000437325.1:n.717+80_717+81del | |
| ENST00000378106.9:c.717+80_717+81del | ENSP00000367346.5:n.717+80_717+81del | |
| ENST00000463598.1:c.633+80_633+81del | ENSP00000420497.1:n.633+80_633+81del | |
| ENST00000464269.5:n.390+80_390+81del | ||
| ENST00000475968.5:n.594+80_594+81del | ||
| ENST00000476124.1:n.117-55_117-54del | ||
| ENST00000476536.5:n.677+80_677+81del | ||
| ENST00000477732.5:n.502+3263_502+3264del | ||
| ENST00000479716.5:n.238+80_238+81del | ||
| ENST00000481249.5:n.594+80_594+81del | ||
| ENST00000485738.5:n.694+80_694+81del | ||
| ENST00000487478.5:n.142-55_142-54del | ||
| NM_001039375.2:c.633+80_633+81del | NP_001034464.1:n.633+80_633+81del | |
| NM_024120.4:c.717+80_717+81del | NP_077025.2:n.717+80_717+81del | |
| NR_029377.1:n.760+80_760+81del | ||
| XM_006723620.2:c.718-55_718-54del | XP_006723683.1:n.718-55_718-54del | |
| XM_006723622.2:c.246+80_246+81del | XP_006723685.1:n.246+80_246+81del | |
| XM_006723623.1:c.246+80_246+81del | XP_006723686.1:n.246+80_246+81del | |
| XM_006723624.1:c.246+80_246+81del | XP_006723687.1:n.246+80_246+81del | |
| XM_011529341.1:c.717+80_717+81del | XP_011527643.1:n.717+80_717+81del | |
| XM_011529342.1:c.717+80_717+81del | XP_011527644.1:n.717+80_717+81del | |
| XM_011529343.1:c.717+80_717+81del | XP_011527645.1:n.717+80_717+81del | |
| XM_011529344.1:c.348+80_348+81del | XP_011527646.1:n.348+80_348+81del | |
| XR_430269.2:n.738-55_738-54del | ||
| XR_937140.1:n.737+80_737+81del | ||
| NM_001352403.1:c.246+80_246+81del | NP_001339332.1:n.246+80_246+81del | |
| NM_001352406.1:c.156+80_156+81del | NP_001339335.1:n.156+80_156+81del | |
| NM_001352407.1:c.156+80_156+81del | NP_001339336.1:n.156+80_156+81del | |
| NM_001352408.1:c.718-55_718-54del | NP_001339337.1:n.718-55_718-54del | |
| NR_147978.1:n.761-55_761-54del | ||
| NR_147979.1:n.780+80_780+81del | ||
| NR_147980.1:n.656+80_656+81del | ||
| NR_147981.1:n.894+80_894+81del | ||
| NR_147982.1:n.895-55_895-54del | ||
| NR_147983.1:n.810+80_810+81del | ||
| XM_006723624.2:c.246+80_246+81del | XP_006723687.1:n.246+80_246+81del | |
| XM_011529342.2:c.717+80_717+81del | XP_011527644.1:n.717+80_717+81del | |
| XM_024451999.1:c.246+80_246+81del | XP_024307767.1:n.246+80_246+81del | |
| XR_001754396.1:n.676+80_676+81del | ||
| XR_430269.3:n.738-55_738-54del | ||
| XR_937140.2:n.737+80_737+81del | ||
| NM_024120.5:c.717+80_717+81del MANE Select | NP_077025.2:n.717+80_717+81del | |
| NM_001039375.3:c.633+80_633+81del | NP_001034464.1:n.633+80_633+81del | |
| NM_001352403.2:c.246+80_246+81del | NP_001339332.1:n.246+80_246+81del | |
| NM_001352406.2:c.156+80_156+81del | NP_001339335.1:n.156+80_156+81del | |
| NM_001352407.2:c.156+80_156+81del | NP_001339336.1:n.156+80_156+81del | |
| NR_029377.2:n.758+80_758+81del | ||
| NR_147978.2:n.759-55_759-54del | ||
| NR_147979.2:n.778+80_778+81del | ||
| NR_147980.2:n.654+80_654+81del | ||
| NR_147981.2:n.892+80_892+81del | ||
| NR_147982.2:n.893-55_893-54del | ||
| NR_147983.2:n.808+80_808+81del | ||
| NM_001352408.2:c.718-55_718-54del | NP_001339337.1:n.718-55_718-54del |