Linked Data
ClinVar Variation Id:
1186822
dbSNP Id:
rs35071801
ExAC:
9:451977 ATTTTTTTTTT / A
gnomAD v2:
9-451977-ATTTTTTTTTT-A
gnomAD v3:
9-451977-ATTTTTTTTTT-A
gnomAD v4:
9-451977-ATTTTTTTTTT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.451993_452002del , CM000671.2:g.451993_452002del | GRCh38 |
| NC_000009.11:g.451993_452002del , CM000671.1:g.451993_452002del | GRCh37 |
| NC_000009.10:g.441993_442002del | NCBI36 |
| NG_017007.1:g.242129_242138del , LRG_196:g.242129_242138del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382329.2:c.5662-18_5662-9del | ENSP00000371766.2:n.5662-18_5662-9del | |
| ENST00000683406.1:n.2437-18_2437-9del | ||
| ENST00000684637.1:n.1643-18_1643-9del | ||
| ENST00000685949.1:n.4750-18_4750-9del | ||
| ENST00000432829.7:c.5962-18_5962-9del MANE Select | ENSP00000394888.3:n.5962-18_5962-9del | |
| ENST00000382329.1:c.4363-18_4363-9del | ENSP00000371766.1:n.4363-18_4363-9del | |
| ENST00000432829.6:c.5962-18_5962-9del | ENSP00000394888.3:n.5962-18_5962-9del | |
| ENST00000453981.5:c.5758-18_5758-9del | ENSP00000408464.2:n.5758-18_5758-9del | |
| ENST00000469391.5:c.5662-18_5662-9del | ENSP00000419438.1:n.5662-18_5662-9del | |
| ENST00000495184.5:n.7917-18_7917-9del | ||
| NM_001190458.1:c.5662-18_5662-9del | NP_001177387.1:n.5662-18_5662-9del | |
| NM_001193536.1:c.5758-18_5758-9del | NP_001180465.1:n.5758-18_5758-9del | |
| NM_203447.3:c.5962-18_5962-9del , LRG_196t1:c.5962-18_5962-9del | NP_982272.2:n.5962-18_5962-9del | |
| XM_011518045.1:c.5662-18_5662-9del | XP_011516347.1:n.5662-18_5662-9del | |
| XM_011518046.1:c.5824-18_5824-9del | XP_011516348.1:n.5824-18_5824-9del | |
| XM_011518047.1:c.5758-18_5758-9del | XP_011516349.1:n.5758-18_5758-9del | |
| XM_011518048.1:c.5758-18_5758-9del | XP_011516350.1:n.5758-18_5758-9del | |
| XM_011518049.1:c.4198-18_4198-9del | XP_011516351.1:n.4198-18_4198-9del | |
| XM_011518045.3:c.5662-18_5662-9del | XP_011516347.1:n.5662-18_5662-9del | |
| XM_011518046.2:c.5824-18_5824-9del | XP_011516348.1:n.5824-18_5824-9del | |
| XM_011518047.3:c.5758-18_5758-9del | XP_011516349.1:n.5758-18_5758-9del | |
| XM_011518048.2:c.5758-18_5758-9del | XP_011516350.1:n.5758-18_5758-9del | |
| XM_011518049.2:c.4198-18_4198-9del | XP_011516351.1:n.4198-18_4198-9del | |
| XM_017015173.1:c.5758-18_5758-9del | XP_016870662.1:n.5758-18_5758-9del | |
| XM_017015174.1:c.5824-18_5824-9del | XP_016870663.1:n.5824-18_5824-9del | |
| NM_001190458.2:c.5662-18_5662-9del | NP_001177387.1:n.5662-18_5662-9del | |
| NM_001193536.2:c.5758-18_5758-9del | NP_001180465.1:n.5758-18_5758-9del | |
| NM_203447.4:c.5962-18_5962-9del MANE Select | NP_982272.2:n.5962-18_5962-9del |