Linked Data
ClinVar Variation Id:
187716
dbSNP Id:
rs786203945
ExAC:
17:56772324 ACT / A
gnomAD v2:
17-56772324-ACT-A
gnomAD v4:
17-58694963-ACT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58694966_58694967del , CM000679.2:g.58694966_58694967del | GRCh38 |
| NC_000017.10:g.56772327_56772328del , CM000679.1:g.56772327_56772328del | GRCh37 |
| NC_000017.9:g.54127326_54127327del | NCBI36 |
| NG_023199.1:g.7365_7366del , LRG_314:g.7365_7366del | |
| NG_047169.1:g.2115_2116del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461271.6:c.-171_-170del | ENSP00000464056.2:n.-171_-170del | |
| ENST00000697675.1:n.1275_1276del | ||
| ENST00000697676.1:n.241_242del | ||
| ENST00000697677.1:n.1262_1263del | ||
| ENST00000697678.1:n.83_84del | ||
| ENST00000697679.1:n.1255_1256del | ||
| ENST00000697680.1:c.*1045_*1046del | ENSP00000513392.1:n.*1045_*1046del | |
| ENST00000697681.1:c.*1045_*1046del | ENSP00000513393.1:n.*1045_*1046del | |
| ENST00000697683.1:c.*1045_*1046del | ENSP00000513395.1:n.*1045_*1046del | |
| ENST00000697684.1:n.241_242del | ||
| ENST00000697685.1:c.*1045_*1046del | ENSP00000513396.1:n.*1045_*1046del | |
| ENST00000697686.1:c.-171_-170del | ENSP00000513397.1:n.-171_-170del | |
| ENST00000697687.1:n.227_228del | ||
| ENST00000697688.1:n.227_228del | ||
| ENST00000697689.1:c.*884_*885del | ENSP00000513398.1:n.*884_*885del | |
| ENST00000697690.1:c.181_182del | ENSP00000513399.1:p.Leu61AlafsTer11 | |
| ENST00000697691.1:c.*153_*154del | ENSP00000513400.1:n.*153_*154del | |
| ENST00000697692.1:c.*193_*194del | ENSP00000513401.1:n.*193_*194del | |
| ENST00000697693.1:n.956_957del | ||
| ENST00000697694.1:c.-171_-170del | ENSP00000513402.1:n.-171_-170del | |
| ENST00000697695.1:n.788_789del | ||
| ENST00000337432.9:c.181_182del MANE Select | ENSP00000336701.4:p.Leu61AlafsTer11 | |
| ENST00000337432.8:c.181_182del | ENSP00000336701.4:p.Leu61AlafsTer11 | |
| ENST00000421782.3:c.181_182del | ENSP00000391450.2:p.Leu61AlafsTer11 | |
| ENST00000461271.5:c.-171_-170del | ENSP00000464056.1:n.-171_-170del | |
| ENST00000475762.5:c.*884_*885del | ENSP00000432421.1:n.*884_*885del | |
| ENST00000482007.5:c.181_182del | ENSP00000433332.1:p.Leu61AlafsTer11 | |
| ENST00000486827.1:c.*1045_*1046del | ENSP00000436761.1:n.*1045_*1046del | |
| ENST00000487525.5:c.181_182del | ENSP00000431637.1:p.Leu61AlafsTer11 | |
| ENST00000487921.5:n.93_94del | ||
| ENST00000583539.5:c.181_182del | ENSP00000463121.1:p.Leu61AlafsTer11 | |
| ENST00000584617.5:c.127-1727_127-1726del | ||
| NM_002876.3:c.181_182del | NP_002867.1:p.Leu61AlafsTer11 | |
| NM_058216.2:c.181_182del | NP_478123.1:p.Leu61AlafsTer11 | |
| NR_103872.1:n.252_253del | ||
| NR_103873.1:n.149_150del | ||
| XM_006722001.2:c.181_182del | XP_006722064.1:p.Leu61AlafsTer11 | |
| XM_006722002.2:c.181_182del | XP_006722065.1:p.Leu61AlafsTer11 | |
| XM_006722004.2:c.-171_-170del | XP_006722067.1:n.-171_-170del | |
| XM_006722005.2:c.-171_-170del | XP_006722068.1:n.-171_-170del | |
| XM_011525092.1:c.-171_-170del | XP_011523394.1:n.-171_-170del | |
| XM_011525093.1:c.-171_-170del | XP_011523395.1:n.-171_-170del | |
| XM_011525094.1:c.-171_-170del | XP_011523396.1:n.-171_-170del | |
| XR_934513.1:n.254_255del | ||
| XR_934514.1:n.254_255del | ||
| XM_006722001.4:c.181_182del | XP_006722064.1:p.Leu61AlafsTer11 | |
| XM_006722002.4:c.181_182del | XP_006722065.1:p.Leu61AlafsTer11 | |
| XM_006722004.3:c.-171_-170del | XP_006722067.1:n.-171_-170del | |
| XM_006722005.3:c.-171_-170del | XP_006722068.1:n.-171_-170del | |
| XM_011525092.2:c.-171_-170del | XP_011523394.1:n.-171_-170del | |
| XM_011525093.2:c.-171_-170del | XP_011523395.1:n.-171_-170del | |
| XM_011525094.2:c.-171_-170del | XP_011523396.1:n.-171_-170del | |
| XM_017024914.1:c.-171_-170del | XP_016880403.1:n.-171_-170del | |
| XM_017024915.1:c.-171_-170del | XP_016880404.1:n.-171_-170del | |
| XM_017024916.1:c.-171_-170del | XP_016880405.1:n.-171_-170del | |
| XM_017024917.1:c.-171_-170del | XP_016880406.1:n.-171_-170del | |
| XM_017024918.2:c.-171_-170del | XP_016880407.1:n.-171_-170del | |
| XM_017024919.1:c.-171_-170del | XP_016880408.1:n.-171_-170del | |
| XR_934513.3:n.685_686del | ||
| XR_934514.3:n.685_686del | ||
| NM_058216.3:c.181_182del MANE Select | NP_478123.1:p.Leu61AlafsTer11 | |
| NR_103872.2:n.223_224del | ||
| NM_002876.4:c.181_182del | NP_002867.1:p.Leu61AlafsTer11 |