Linked Data
ClinVar Variation Id:
409860
ClinVar RCV Id:
RCV003316570
dbSNP Id:
rs1060502601
gnomAD v4:
17-58709883-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58709885del , CM000679.2:g.58709885del | GRCh38 |
| NC_000017.10:g.56787246del , CM000679.1:g.56787246del | GRCh37 |
| NC_000017.9:g.54142245del | NCBI36 |
| NG_023199.1:g.22284del , LRG_314:g.22284del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461271.6:c.381del | ENSP00000464056.2:p.Ile127MetfsTer9 | |
| ENST00000697678.1:n.634del | ||
| ENST00000697679.1:n.1806del | ||
| ENST00000697680.1:c.*1596del | ENSP00000513392.1:n.*1596del | |
| ENST00000697681.1:c.*1893del | ENSP00000513393.1:n.*1893del | |
| ENST00000697683.1:c.*1596del | ENSP00000513395.1:n.*1596del | |
| ENST00000697684.1:n.792del | ||
| ENST00000697685.1:c.*1429del | ENSP00000513396.1:n.*1429del | |
| ENST00000697686.1:c.381del | ENSP00000513397.1:p.Ile127MetfsTer9 | |
| ENST00000697687.1:n.611del | ||
| ENST00000697688.1:n.778del | ||
| ENST00000697689.1:c.*1268del | ENSP00000513398.1:n.*1268del | |
| ENST00000697690.1:c.732del | ENSP00000513399.1:p.Ile244MetfsTer9 | |
| ENST00000697691.1:c.*704del | ENSP00000513400.1:n.*704del | |
| ENST00000697692.1:c.*744del | ENSP00000513401.1:n.*744del | |
| ENST00000697694.1:c.381del | ENSP00000513402.1:p.Ile127MetfsTer9 | |
| ENST00000697695.1:n.1339del | ||
| ENST00000337432.9:c.732del MANE Select | ENSP00000336701.4:p.Ile244MetfsTer9 | |
| ENST00000337432.8:c.732del | ENSP00000336701.4:p.Ile244MetfsTer9 | |
| ENST00000413590.5:c.370del | ||
| ENST00000461271.5:c.381del | ENSP00000464056.1:p.Ile127MetfsTer9 | |
| ENST00000475762.5:c.*1435del | ENSP00000432421.1:n.*1435del | |
| ENST00000482007.5:c.*160del | ENSP00000433332.1:n.*160del | |
| ENST00000487525.5:c.*305del | ENSP00000431637.1:n.*305del | |
| ENST00000578151.1:n.67del | ||
| ENST00000581221.5:n.247del | ||
| ENST00000583539.5:c.732del | ENSP00000463121.1:p.Ile244MetfsTer9 | |
| ENST00000584617.5:c.454del | ||
| ENST00000584804.1:c.27del | ENSP00000463658.1:p.Ile9MetfsTer9 | |
| NM_058216.2:c.732del | NP_478123.1:p.Ile244MetfsTer9 | |
| NR_103872.1:n.636del | ||
| XM_006722001.2:c.732del | XP_006722064.1:p.Ile244MetfsTer9 | |
| XM_006722002.2:c.732del | XP_006722065.1:p.Ile244MetfsTer9 | |
| XM_006722004.2:c.381del | XP_006722067.1:p.Ile127MetfsTer9 | |
| XM_006722005.2:c.381del | XP_006722068.1:p.Ile127MetfsTer9 | |
| XM_011525092.1:c.381del | XP_011523394.1:p.Ile127MetfsTer9 | |
| XM_011525093.1:c.381del | XP_011523395.1:p.Ile127MetfsTer9 | |
| XM_011525094.1:c.381del | XP_011523396.1:p.Ile127MetfsTer9 | |
| XR_934513.1:n.950del | ||
| XR_934514.1:n.950del | ||
| XM_006722001.4:c.732del | XP_006722064.1:p.Ile244MetfsTer9 | |
| XM_006722002.4:c.732del | XP_006722065.1:p.Ile244MetfsTer9 | |
| XM_006722004.3:c.381del | XP_006722067.1:p.Ile127MetfsTer9 | |
| XM_006722005.3:c.381del | XP_006722068.1:p.Ile127MetfsTer9 | |
| XM_011525092.2:c.381del | XP_011523394.1:p.Ile127MetfsTer9 | |
| XM_011525093.2:c.381del | XP_011523395.1:p.Ile127MetfsTer9 | |
| XM_011525094.2:c.381del | XP_011523396.1:p.Ile127MetfsTer9 | |
| XM_017024914.1:c.381del | XP_016880403.1:p.Ile127MetfsTer9 | |
| XM_017024915.1:c.381del | XP_016880404.1:p.Ile127MetfsTer9 | |
| XM_017024916.1:c.381del | XP_016880405.1:p.Ile127MetfsTer9 | |
| XM_017024917.1:c.381del | XP_016880406.1:p.Ile127MetfsTer9 | |
| XM_017024918.2:c.381del | XP_016880407.1:p.Ile127MetfsTer9 | |
| XM_017024919.1:c.381del | XP_016880408.1:p.Ile127MetfsTer9 | |
| XR_934513.3:n.1381del | ||
| XR_934514.3:n.1381del | ||
| NM_058216.3:c.732del MANE Select | NP_478123.1:p.Ile244MetfsTer9 | |
| NR_103872.2:n.607del |