Linked Data
ClinVar Variation Id:
201572
dbSNP Id:
rs749697698
ExAC:
3:38593010 GAGA / G
gnomAD v2:
3-38593010-GAGA-G
gnomAD v4:
3-38551519-GAGA-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.38551525_38551527del , CM000665.2:g.38551525_38551527del | GRCh38 |
| NC_000003.11:g.38593016_38593018del , CM000665.1:g.38593016_38593018del | GRCh37 |
| NC_000003.10:g.38568020_38568022del | NCBI36 |
| NG_008934.1:g.103151_103153del , LRG_289:g.103151_103153del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000327956.7:c.4847_4849del | ENSP00000333674.7:p.Phe1616del | |
| ENST00000333535.9:c.4850_4852del | ENSP00000328968.4:p.Phe1617del | |
| ENST00000413689.6:c.4850_4852del MANE Plus Clinical | ENSP00000410257.1:p.Phe1617del | |
| ENST00000423572.7:c.4847_4849del MANE Select | ENSP00000398266.2:p.Phe1616del | |
| ENST00000333535.8:c.4850_4852del | ENSP00000328968.4:p.Phe1617del | |
| ENST00000413689.5:c.4850_4852del | ENSP00000410257.1:p.Phe1617del | |
| ENST00000414099.6:c.4796_4798del | ENSP00000398962.2:p.Phe1599del | |
| ENST00000423572.6:c.4847_4849del | ENSP00000398266.2:p.Phe1616del | |
| ENST00000425664.5:c.4796_4798del | ENSP00000416634.1:p.Phe1599del | |
| ENST00000449557.6:c.4688_4690del | ENSP00000413996.2:p.Phe1563del | |
| ENST00000450102.6:c.4688_4690del | ENSP00000403355.2:p.Phe1563del | |
| ENST00000451551.6:c.4688_4690del | ENSP00000388797.2:p.Phe1563del | |
| ENST00000455624.6:c.4751_4753del | ENSP00000399524.2:p.Phe1584del | |
| NM_000335.4:c.4847_4849del , LRG_289t2:c.4847_4849del | NP_000326.2:p.Phe1616del | |
| NM_001099404.1:c.4850_4852del , LRG_289t3:c.4850_4852del | NP_001092874.1:p.Phe1617del | |
| NM_001099405.1:c.4796_4798del | NP_001092875.1:p.Phe1599del | |
| NM_001160160.1:c.4751_4753del | NP_001153632.1:p.Phe1584del | |
| NM_001160161.1:c.4688_4690del | NP_001153633.1:p.Phe1563del | |
| NM_198056.2:c.4850_4852del , LRG_289t1:c.4850_4852del | NP_932173.1:p.Phe1617del | |
| XM_006713282.2:c.4850_4852del | XP_006713345.1:p.Phe1617del | |
| XM_011533991.1:c.4847_4849del | XP_011532293.1:p.Phe1616del | |
| XM_011533992.1:c.4721_4723del | XP_011532294.1:p.Phe1574del | |
| NM_001354701.1:c.4793_4795del | NP_001341630.1:p.Phe1598del | |
| XM_011533991.2:c.4847_4849del | XP_011532293.1:p.Phe1616del | |
| XM_017007017.1:c.4688_4690del | XP_016862506.1:p.Phe1563del | |
| NM_000335.5:c.4847_4849del MANE Select | NP_000326.2:p.Phe1616del | |
| NM_001160160.2:c.4751_4753del | NP_001153632.1:p.Phe1584del | |
| NM_001354701.2:c.4793_4795del | NP_001341630.1:p.Phe1598del | |
| NM_001099404.2:c.4850_4852del MANE Plus Clinical | NP_001092874.1:p.Phe1617del | |
| NM_001099405.2:c.4796_4798del | NP_001092875.1:p.Phe1599del | |
| NM_001160161.2:c.4688_4690del | NP_001153633.1:p.Phe1563del | |
| NM_198056.3:c.4850_4852del | NP_932173.1:p.Phe1617del |