Linked Data
ClinVar Variation Id:
54743
dbSNP Id:
rs80358333
ExAC:
17:41244544 TTTCCTC / T
gnomAD v2:
17-41244544-TTTCCTC-T
gnomAD v3:
17-43092527-TTTCCTC-T
gnomAD v4:
17-43092527-TTTCCTC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43092529_43092534del , CM000679.2:g.43092529_43092534del | GRCh38 |
| NC_000017.10:g.41244546_41244551del , CM000679.1:g.41244546_41244551del | GRCh37 |
| NC_000017.9:g.38498072_38498077del | NCBI36 |
| NG_005905.2:g.125451_125456del , LRG_292:g.125451_125456del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3062_3067del | ||
| ENST00000461574.2:c.2998_3003del | ENSP00000417241.2:p.Glu1000_Glu1001del | |
| ENST00000470026.6:c.2998_3003del | ENSP00000419274.2:p.Glu1000_Glu1001del | |
| ENST00000473961.6:c.2872_2877del | ENSP00000420201.2:p.Glu958_Glu959del | |
| ENST00000476777.6:c.2995_3000del | ENSP00000417554.2:p.Glu999_Glu1000del | |
| ENST00000477152.6:c.2920_2925del | ENSP00000419988.2:p.Glu974_Glu975del | |
| ENST00000478531.6:c.785-1501_785-1496del | ENSP00000420412.2:n.785-1501_785-1496del | |
| ENST00000489037.2:c.2920_2925del | ENSP00000420781.2:p.Glu974_Glu975del | |
| ENST00000493919.6:c.647-1501_647-1496del | ENSP00000418819.2:n.647-1501_647-1496del | |
| ENST00000494123.6:c.2998_3003del | ENSP00000419103.2:p.Glu1000_Glu1001del | |
| ENST00000497488.2:c.2110_2115del | ENSP00000418986.2:p.Glu704_Glu705del | |
| ENST00000618469.2:c.2998_3003del | ENSP00000478114.2:p.Glu1000_Glu1001del | |
| ENST00000634433.2:c.2875_2880del | ENSP00000489431.2:p.Glu959_Glu960del | |
| ENST00000644379.2:c.2998_3003del | ENSP00000496570.2:p.Glu1000_Glu1001del | |
| ENST00000644555.2:c.647-1501_647-1496del | ENSP00000494614.2:n.647-1501_647-1496del | |
| ENST00000652672.2:c.2857_2862del | ENSP00000498906.2:p.Glu953_Glu954del | |
| ENST00000484087.6:c.665-1501_665-1496del | ENSP00000419481.2:n.665-1501_665-1496del | |
| ENST00000700182.1:c.707-1501_707-1496del | ENSP00000514849.1:n.707-1501_707-1496del | |
| ENST00000357654.9:c.2998_3003del MANE Select | ENSP00000350283.3:p.Glu1000_Glu1001del | |
| ENST00000471181.7:c.2998_3003del | ENSP00000418960.2:p.Glu1000_Glu1001del | |
| ENST00000352993.7:c.671-1501_671-1496del | ENSP00000312236.5:n.671-1501_671-1496del | |
| ENST00000354071.7:c.2998_3003del | ENSP00000326002.7:p.Glu1000_Glu1001del | |
| ENST00000357654.7:c.2998_3003del | ENSP00000350283.3:p.Glu1000_Glu1001del | |
| ENST00000461221.5:c.*2781_*2786del | ENSP00000418548.1:n.*2781_*2786del | |
| ENST00000468300.5:c.788-1501_788-1496del | ENSP00000417148.1:n.788-1501_788-1496del | |
| ENST00000471181.6:c.2998_3003del | ENSP00000418960.2:p.Glu1000_Glu1001del | |
| ENST00000478531.5:c.785-1501_785-1496del | ENSP00000420412.1:n.785-1501_785-1496del | |
| ENST00000484087.5:c.410-1501_410-1496del | ENSP00000419481.1:n.410-1501_410-1496del | |
| ENST00000487825.5:c.413-1501_413-1496del | ENSP00000418212.1:n.413-1501_413-1496del | |
| ENST00000491747.6:c.788-1501_788-1496del | ENSP00000420705.2:n.788-1501_788-1496del | |
| ENST00000493795.5:c.2857_2862del | ENSP00000418775.1:p.Glu953_Glu954del | |
| ENST00000493919.5:c.647-1501_647-1496del | ENSP00000418819.1:n.647-1501_647-1496del | |
| ENST00000586385.5:c.5-28582_5-28577del | ENSP00000465818.1:n.5-28582_5-28577del | |
| ENST00000591534.5:c.-43-18012_-43-18007del | ENSP00000467329.1:n.-43-18012_-43-18007del | |
| ENST00000591849.5:c.-99+32738_-99+32743del | ENSP00000465347.1:n.-99+32738_-99+32743del | |
| NM_007294.3:c.2998_3003del , LRG_292t1:c.2998_3003del | NP_009225.1:p.Glu1000_Glu1001del | |
| NM_007297.3:c.2857_2862del | NP_009228.2:p.Glu953_Glu954del | |
| NM_007298.3:c.788-1501_788-1496del | NP_009229.2:n.788-1501_788-1496del | |
| NM_007299.3:c.788-1501_788-1496del | NP_009230.2:n.788-1501_788-1496del | |
| NM_007300.3:c.2998_3003del | NP_009231.2:p.Glu1000_Glu1001del | |
| NR_027676.1:n.3134_3139del | ||
| NM_007294.4:c.2998_3003del MANE Select | NP_009225.1:p.Glu1000_Glu1001del | |
| NM_007297.4:c.2857_2862del | NP_009228.2:p.Glu953_Glu954del | |
| NM_007299.4:c.788-1501_788-1496del | NP_009230.2:n.788-1501_788-1496del | |
| NM_007300.4:c.2998_3003del | NP_009231.2:p.Glu1000_Glu1001del | |
| NR_027676.2:n.3175_3180del |