Linked Data
ClinVar Variation Id:
1442079
dbSNP Id:
rs763110421
gnomAD v2:
17-41244386-CACTTCATTAGTACTGGAACCT-C
gnomAD v4:
17-43092369-CACTTCATTAGTACTGGAACCT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43092379_43092399del , CM000679.2:g.43092379_43092399del | GRCh38 |
| NC_000017.10:g.41244396_41244416del , CM000679.1:g.41244396_41244416del | GRCh37 |
| NC_000017.9:g.38497922_38497942del | NCBI36 |
| NG_005905.2:g.125594_125614del , LRG_292:g.125594_125614del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.3205_3225del | ||
| ENST00000461574.2:c.3141_3161del | ENSP00000417241.2:p.Gly1048_Val1054del | |
| ENST00000470026.6:c.3141_3161del | ENSP00000419274.2:p.Gly1048_Val1054del | |
| ENST00000473961.6:c.3015_3035del | ENSP00000420201.2:p.Gly1006_Val1012del | |
| ENST00000476777.6:c.3138_3158del | ENSP00000417554.2:p.Gly1047_Val1053del | |
| ENST00000477152.6:c.3063_3083del | ENSP00000419988.2:p.Gly1022_Val1028del | |
| ENST00000478531.6:c.785-1358_785-1338del | ENSP00000420412.2:n.785-1358_785-1338del | |
| ENST00000489037.2:c.3063_3083del | ENSP00000420781.2:p.Gly1022_Val1028del | |
| ENST00000493919.6:c.647-1358_647-1338del | ENSP00000418819.2:n.647-1358_647-1338del | |
| ENST00000494123.6:c.3141_3161del | ENSP00000419103.2:p.Gly1048_Val1054del | |
| ENST00000497488.2:c.2253_2273del | ENSP00000418986.2:p.Gly752_Val758del | |
| ENST00000618469.2:c.3141_3161del | ENSP00000478114.2:p.Gly1048_Val1054del | |
| ENST00000634433.2:c.3018_3038del | ENSP00000489431.2:p.Gly1007_Val1013del | |
| ENST00000644379.2:c.3141_3161del | ENSP00000496570.2:p.Gly1048_Val1054del | |
| ENST00000644555.2:c.647-1358_647-1338del | ENSP00000494614.2:n.647-1358_647-1338del | |
| ENST00000652672.2:c.3000_3020del | ENSP00000498906.2:p.Gly1001_Val1007del | |
| ENST00000484087.6:c.665-1358_665-1338del | ENSP00000419481.2:n.665-1358_665-1338del | |
| ENST00000700182.1:c.707-1358_707-1338del | ENSP00000514849.1:n.707-1358_707-1338del | |
| ENST00000357654.9:c.3141_3161del MANE Select | ENSP00000350283.3:p.Gly1048_Val1054del | |
| ENST00000471181.7:c.3141_3161del | ENSP00000418960.2:p.Gly1048_Val1054del | |
| ENST00000352993.7:c.671-1358_671-1338del | ENSP00000312236.5:n.671-1358_671-1338del | |
| ENST00000354071.7:c.3141_3161del | ENSP00000326002.7:p.Gly1048_Val1054del | |
| ENST00000357654.7:c.3141_3161del | ENSP00000350283.3:p.Gly1048_Val1054del | |
| ENST00000461221.5:c.*2924_*2944del | ENSP00000418548.1:n.*2924_*2944del | |
| ENST00000468300.5:c.788-1358_788-1338del | ENSP00000417148.1:n.788-1358_788-1338del | |
| ENST00000471181.6:c.3141_3161del | ENSP00000418960.2:p.Gly1048_Val1054del | |
| ENST00000478531.5:c.785-1358_785-1338del | ENSP00000420412.1:n.785-1358_785-1338del | |
| ENST00000484087.5:c.410-1358_410-1338del | ENSP00000419481.1:n.410-1358_410-1338del | |
| ENST00000487825.5:c.413-1358_413-1338del | ENSP00000418212.1:n.413-1358_413-1338del | |
| ENST00000491747.6:c.788-1358_788-1338del | ENSP00000420705.2:n.788-1358_788-1338del | |
| ENST00000493795.5:c.3000_3020del | ENSP00000418775.1:p.Gly1001_Val1007del | |
| ENST00000493919.5:c.647-1358_647-1338del | ENSP00000418819.1:n.647-1358_647-1338del | |
| ENST00000586385.5:c.5-28439_5-28419del | ENSP00000465818.1:n.5-28439_5-28419del | |
| ENST00000591534.5:c.-43-17869_-43-17849del | ENSP00000467329.1:n.-43-17869_-43-17849del | |
| ENST00000591849.5:c.-99+32881_-99+32901del | ENSP00000465347.1:n.-99+32881_-99+32901del | |
| NM_007294.3:c.3141_3161del , LRG_292t1:c.3141_3161del | NP_009225.1:p.Gly1048_Val1054del | |
| NM_007297.3:c.3000_3020del | NP_009228.2:p.Gly1001_Val1007del | |
| NM_007298.3:c.788-1358_788-1338del | NP_009229.2:n.788-1358_788-1338del | |
| NM_007299.3:c.788-1358_788-1338del | NP_009230.2:n.788-1358_788-1338del | |
| NM_007300.3:c.3141_3161del | NP_009231.2:p.Gly1048_Val1054del | |
| NR_027676.1:n.3277_3297del | ||
| NM_007294.4:c.3141_3161del MANE Select | NP_009225.1:p.Gly1048_Val1054del | |
| NM_007297.4:c.3000_3020del | NP_009228.2:p.Gly1001_Val1007del | |
| NM_007299.4:c.788-1358_788-1338del | NP_009230.2:n.788-1358_788-1338del | |
| NM_007300.4:c.3141_3161del | NP_009231.2:p.Gly1048_Val1054del | |
| NR_027676.2:n.3318_3338del |