Linked Data
dbSNP Id:
rs778853261
ExAC:
X:38144916 CTG / C
gnomAD v2:
X-38144916-CTG-C
gnomAD v4:
X-38285663-CTG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38285669_38285670del , CM000685.2:g.38285669_38285670del | GRCh38 |
| NC_000023.10:g.38144922_38144923del , CM000685.1:g.38144922_38144923del | GRCh37 |
| NC_000023.9:g.38029866_38029867del | NCBI36 |
| NG_009553.1:g.46871_46872del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494707.6:c.953+2200_953+2201del | ||
| ENST00000642170.1:n.1826+5294_1826+5295del | ||
| ENST00000642395.2:c.1905+1429_1905+1430del | ENSP00000493468.2:n.1905+1429_1905+1430del | |
| ENST00000642739.1:c.1572+5294_1572+5295del | ENSP00000493596.1:n.1572+5294_1572+5295del | |
| ENST00000644238.1:c.1386+5294_1386+5295del | ENSP00000496728.1:n.1386+5294_1386+5295del | |
| ENST00000644337.1:c.1719+1429_1719+1430del | ENSP00000494557.1:n.1719+1429_1719+1430del | |
| ENST00000645032.1:c.3334_3335del MANE Select | ENSP00000495537.1:p.Gln1112GlyfsTer? | |
| ENST00000645124.1:c.*101+1429_*101+1430del | ENSP00000496446.1:n.*101+1429_*101+1430del | |
| ENST00000646020.1:c.*594+1429_*594+1430del | ENSP00000494745.1:n.*594+1429_*594+1430del | |
| ENST00000318842.11:c.1905+1429_1905+1430del | ENSP00000322219.6:n.1905+1429_1905+1430del | |
| ENST00000339363.7:c.2520+1429_2520+1430del | ENSP00000343671.3:n.2520+1429_2520+1430del | |
| ENST00000378505.6:c.3334_3335del | ENSP00000367766.2:p.Gln1112GlyfsTer? | |
| ENST00000465127.1:c.172-380452_172-380451del | ENSP00000417050.1:n.172-380452_172-380451del | |
| ENST00000474584.5:c.*37+5294_*37+5295del | ENSP00000418926.1:n.*37+5294_*37+5295del | |
| ENST00000482855.5:c.1905+1429_1905+1430del | ENSP00000419276.1:n.1905+1429_1905+1430del | |
| ENST00000494707.5:c.139+5294_139+5295del | ||
| NM_000328.2:c.1905+1429_1905+1430del | NP_000319.1:n.1905+1429_1905+1430del | |
| NM_001034853.1:c.3334_3335del | NP_001030025.1:p.Gln1112GlyfsTer? | |
| XM_005272633.1:c.1572+5294_1572+5295del | XP_005272690.1:n.1572+5294_1572+5295del | |
| XM_011543940.1:c.1902+1429_1902+1430del | XP_011542242.1:n.1902+1429_1902+1430del | |
| XM_005272633.3:c.1572+5294_1572+5295del | XP_005272690.1:n.1572+5294_1572+5295del | |
| XM_011543940.3:c.1902+1429_1902+1430del | XP_011542242.1:n.1902+1429_1902+1430del | |
| XM_017029712.2:c.1569+5294_1569+5295del | XP_016885201.1:n.1569+5294_1569+5295del | |
| NM_001367245.1:c.1902+1429_1902+1430del | NP_001354174.1:n.1902+1429_1902+1430del | |
| NM_001367246.1:c.1719+1429_1719+1430del | NP_001354175.1:n.1719+1429_1719+1430del | |
| NM_001367247.1:c.1572+5294_1572+5295del | NP_001354176.1:n.1572+5294_1572+5295del | |
| NM_001367248.1:c.1602+5294_1602+5295del | NP_001354177.1:n.1602+5294_1602+5295del | |
| NM_001367249.1:c.1569+5294_1569+5295del | NP_001354178.1:n.1569+5294_1569+5295del | |
| NM_001367250.1:c.1569+5294_1569+5295del | NP_001354179.1:n.1569+5294_1569+5295del | |
| NM_001367251.1:c.1386+5294_1386+5295del | NP_001354180.1:n.1386+5294_1386+5295del | |
| NR_159803.1:n.2263+1429_2263+1430del | ||
| NR_159804.1:n.1648+5294_1648+5295del | ||
| NR_159805.1:n.1714+5294_1714+5295del | ||
| NR_159806.1:n.1866+1429_1866+1430del | ||
| NR_159807.1:n.1622+5294_1622+5295del | ||
| NR_159808.1:n.1826+5294_1826+5295del | ||
| NM_000328.3:c.1905+1429_1905+1430del | NP_000319.1:n.1905+1429_1905+1430del | |
| NM_001034853.2:c.3334_3335del MANE Select | NP_001030025.1:p.Gln1112GlyfsTer? |