Linked Data
ClinVar Variation Id:
2195891
ClinVar RCV Id:
RCV002633246
dbSNP Id:
rs1193509492
gnomAD v3:
X-38286395-CTCCCCTTCTCCTTCT-C
gnomAD v4:
X-38286395-CTCCCCTTCTCCTTCT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38286405_38286419del , CM000685.2:g.38286405_38286419del | GRCh38 |
| NC_000023.10:g.38145658_38145672del , CM000685.1:g.38145658_38145672del | GRCh37 |
| NC_000023.9:g.38030602_38030616del | NCBI36 |
| NG_009553.1:g.46126_46140del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494707.6:c.953+1455_953+1469del | ||
| ENST00000642170.1:n.1826+4549_1826+4563del | ||
| ENST00000642395.2:c.1905+684_1905+698del | ENSP00000493468.2:n.1905+684_1905+698del | |
| ENST00000642739.1:c.1572+4549_1572+4563del | ENSP00000493596.1:n.1572+4549_1572+4563del | |
| ENST00000644238.1:c.1386+4549_1386+4563del | ENSP00000496728.1:n.1386+4549_1386+4563del | |
| ENST00000644337.1:c.1719+684_1719+698del | ENSP00000494557.1:n.1719+684_1719+698del | |
| ENST00000645032.1:c.2589_2603del MANE Select | ENSP00000495537.1:p.Glu864_Glu868del | |
| ENST00000645124.1:c.*101+684_*101+698del | ENSP00000496446.1:n.*101+684_*101+698del | |
| ENST00000646020.1:c.*594+684_*594+698del | ENSP00000494745.1:n.*594+684_*594+698del | |
| ENST00000318842.11:c.1905+684_1905+698del | ENSP00000322219.6:n.1905+684_1905+698del | |
| ENST00000339363.7:c.2520+684_2520+698del | ENSP00000343671.3:n.2520+684_2520+698del | |
| ENST00000378505.6:c.2589_2603del | ENSP00000367766.2:p.Glu864_Glu868del | |
| ENST00000465127.1:c.172-379716_172-379702del | ENSP00000417050.1:n.172-379716_172-379702del | |
| ENST00000474584.5:c.*37+4549_*37+4563del | ENSP00000418926.1:n.*37+4549_*37+4563del | |
| ENST00000482855.5:c.1905+684_1905+698del | ENSP00000419276.1:n.1905+684_1905+698del | |
| ENST00000494707.5:c.139+4549_139+4563del | ||
| NM_000328.2:c.1905+684_1905+698del | NP_000319.1:n.1905+684_1905+698del | |
| NM_001034853.1:c.2589_2603del | NP_001030025.1:p.Glu864_Glu868del | |
| XM_005272633.1:c.1572+4549_1572+4563del | XP_005272690.1:n.1572+4549_1572+4563del | |
| XM_011543940.1:c.1902+684_1902+698del | XP_011542242.1:n.1902+684_1902+698del | |
| XM_005272633.3:c.1572+4549_1572+4563del | XP_005272690.1:n.1572+4549_1572+4563del | |
| XM_011543940.3:c.1902+684_1902+698del | XP_011542242.1:n.1902+684_1902+698del | |
| XM_017029712.2:c.1569+4549_1569+4563del | XP_016885201.1:n.1569+4549_1569+4563del | |
| NM_001367245.1:c.1902+684_1902+698del | NP_001354174.1:n.1902+684_1902+698del | |
| NM_001367246.1:c.1719+684_1719+698del | NP_001354175.1:n.1719+684_1719+698del | |
| NM_001367247.1:c.1572+4549_1572+4563del | NP_001354176.1:n.1572+4549_1572+4563del | |
| NM_001367248.1:c.1602+4549_1602+4563del | NP_001354177.1:n.1602+4549_1602+4563del | |
| NM_001367249.1:c.1569+4549_1569+4563del | NP_001354178.1:n.1569+4549_1569+4563del | |
| NM_001367250.1:c.1569+4549_1569+4563del | NP_001354179.1:n.1569+4549_1569+4563del | |
| NM_001367251.1:c.1386+4549_1386+4563del | NP_001354180.1:n.1386+4549_1386+4563del | |
| NR_159803.1:n.2263+684_2263+698del | ||
| NR_159804.1:n.1648+4549_1648+4563del | ||
| NR_159805.1:n.1714+4549_1714+4563del | ||
| NR_159806.1:n.1866+684_1866+698del | ||
| NR_159807.1:n.1622+4549_1622+4563del | ||
| NR_159808.1:n.1826+4549_1826+4563del | ||
| NM_000328.3:c.1905+684_1905+698del | NP_000319.1:n.1905+684_1905+698del | |
| NM_001034853.2:c.2589_2603del MANE Select | NP_001030025.1:p.Glu864_Glu868del |