Linked Data
ClinVar Variation Id:
56657
dbSNP Id:
rs180177358
gnomAD v4:
8-99384317-GGT-G
PubMed:
PMID:16648375
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99384318_99384319del , CM000670.2:g.99384318_99384319del | GRCh38 |
| NC_000008.10:g.100396546_100396547del , CM000670.1:g.100396546_100396547del | GRCh37 |
| NC_000008.9:g.100465722_100465723del | NCBI36 |
| NG_007098.2:g.376053_376054del , LRG_351:g.376053_376054del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355155.6:c.2934+1_2934+2del | ENSP00000347281.2:n.2934+1_2934+2del | |
| ENST00000682145.1:n.2811+1_2811+2del | ||
| ENST00000682153.1:c.2934+1_2934+2del | ENSP00000507923.1:n.2934+1_2934+2del | |
| ENST00000682234.1:c.2934+1_2934+2del | ENSP00000508225.1:n.2934+1_2934+2del | |
| ENST00000682358.1:n.3004+1_3004+2del | ||
| ENST00000683334.1:c.2934+1_2934+2del | ENSP00000507369.1:n.2934+1_2934+2del | |
| ENST00000683486.1:n.3000+1_3000+2del | ||
| ENST00000683619.1:n.3106+1_3106+2del | ||
| ENST00000683869.1:n.3015+1_3015+2del | ||
| ENST00000357162.7:c.2934+1_2934+2del MANE Select | ENSP00000349685.2:n.2934+1_2934+2del | |
| ENST00000358544.7:c.2934+1_2934+2del MANE Plus Clinical | ENSP00000351346.2:n.2934+1_2934+2del | |
| ENST00000357162.6:c.2934+1_2934+2del | ENSP00000349685.2:n.2934+1_2934+2del | |
| ENST00000358544.6:c.2934+1_2934+2del | ENSP00000351346.2:n.2934+1_2934+2del | |
| ENST00000496144.5:c.2934+1_2934+2del | ENSP00000430900.1:n.2934+1_2934+2del | |
| ENST00000522802.5:n.156+1_156+2del | ||
| NM_017890.4:c.2934+1_2934+2del , LRG_351t1:c.2934+1_2934+2del | NP_060360.3:n.2934+1_2934+2del | |
| NM_152564.4:c.2934+1_2934+2del , LRG_351t2:c.2934+1_2934+2del | NP_689777.3:n.2934+1_2934+2del | |
| XM_005250800.2:c.2934+1_2934+2del | XP_005250857.1:n.2934+1_2934+2del | |
| XM_005250801.3:c.2934+1_2934+2del | XP_005250858.1:n.2934+1_2934+2del | |
| XM_006716510.2:c.2934+1_2934+2del | XP_006716573.1:n.2934+1_2934+2del | |
| XM_011516848.1:c.2934+1_2934+2del | XP_011515150.1:n.2934+1_2934+2del | |
| XM_011516849.1:c.2934+1_2934+2del | XP_011515151.1:n.2934+1_2934+2del | |
| XM_011516850.1:c.2556+1_2556+2del | XP_011515152.1:n.2556+1_2556+2del | |
| XM_011516853.1:c.2934+1_2934+2del | XP_011515155.1:n.2934+1_2934+2del | |
| XM_011516855.1:c.2934+1_2934+2del | XP_011515157.1:n.2934+1_2934+2del | |
| XM_011516856.1:c.2934+1_2934+2del | XP_011515158.1:n.2934+1_2934+2del | |
| XM_011516857.1:c.2934+1_2934+2del | XP_011515159.1:n.2934+1_2934+2del | |
| XM_011516858.1:c.2934+1_2934+2del | XP_011515160.1:n.2934+1_2934+2del | |
| XM_011516859.1:c.2934+1_2934+2del | XP_011515161.1:n.2934+1_2934+2del | |
| XM_011516860.1:c.2934+1_2934+2del | XP_011515162.1:n.2934+1_2934+2del | |
| XM_011516861.1:c.2934+1_2934+2del | XP_011515163.1:n.2934+1_2934+2del | |
| XR_928301.1:n.3037+1_3037+2del | ||
| XR_928302.1:n.3037+1_3037+2del | ||
| XR_928303.1:n.3037+1_3037+2del | ||
| XR_928304.1:n.3037+1_3037+2del | ||
| XM_005250800.3:c.2934+1_2934+2del | XP_005250857.1:n.2934+1_2934+2del | |
| XM_005250801.5:c.2934+1_2934+2del | XP_005250858.1:n.2934+1_2934+2del | |
| XM_006716510.3:c.2934+1_2934+2del | XP_006716573.1:n.2934+1_2934+2del | |
| XM_011516848.2:c.2934+1_2934+2del | XP_011515150.1:n.2934+1_2934+2del | |
| XM_011516849.2:c.2934+1_2934+2del | XP_011515151.1:n.2934+1_2934+2del | |
| XM_011516850.2:c.2556+1_2556+2del | XP_011515152.1:n.2556+1_2556+2del | |
| XM_011516853.2:c.2934+1_2934+2del | XP_011515155.1:n.2934+1_2934+2del | |
| XM_011516859.2:c.2934+1_2934+2del | XP_011515161.1:n.2934+1_2934+2del | |
| XM_017013109.1:c.2739+1_2739+2del | XP_016868598.1:n.2739+1_2739+2del | |
| XM_024447074.1:c.1719+1_1719+2del | XP_024302842.1:n.1719+1_1719+2del | |
| XM_024447075.1:c.2934+1_2934+2del | XP_024302843.1:n.2934+1_2934+2del | |
| XR_001745481.1:n.3037+1_3037+2del | ||
| XR_001745482.2:n.3037+1_3037+2del | ||
| XR_001745484.2:n.3037+1_3037+2del | ||
| XR_002956601.1:n.3037+1_3037+2del | ||
| XR_002956602.1:n.3037+1_3037+2del | ||
| XR_928302.2:n.3037+1_3037+2del | ||
| NM_017890.5:c.2934+1_2934+2del MANE Plus Clinical | NP_060360.3:n.2934+1_2934+2del | |
| NM_152564.5:c.2934+1_2934+2del MANE Select | NP_689777.3:n.2934+1_2934+2del |