Linked Data
ClinVar Variation Id:
4536
dbSNP Id:
rs786205071
gnomAD v2:
11-62462152-G-GT
gnomAD v3:
11-62694680-G-GT
gnomAD v4:
11-62694680-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62694681dup , CM000673.2:g.62694681dup | GRCh38 |
| NC_000011.9:g.62462153dup , CM000673.1:g.62462153dup | GRCh37 |
| NC_000011.8:g.62218729dup | NCBI36 |
| NG_008461.1:g.19894dup | |
| NG_033077.1:g.219dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412351.2:n.709dup (BSCL2) | ||
| ENST00000449636.6:c.25dup (BSCL2) | ENSP00000405265.2:p.Thr9AsnfsTer5 | |
| ENST00000524862.6:c.517dup (BSCL2) | ENSP00000433888.2:p.Thr173AsnfsTer5 | |
| ENST00000682003.1:n.695dup (BSCL2) | ||
| ENST00000682223.1:c.517dup (BSCL2) | ENSP00000508140.1:p.Thr173AsnfsTer5 | |
| ENST00000682262.1:c.517dup (BSCL2) | ENSP00000507103.1:p.Thr173AsnfsTer5 | |
| ENST00000682555.1:c.517dup (BSCL2) | ENSP00000507814.1:p.Thr173AsnfsTer5 | |
| ENST00000682644.1:n.909dup (BSCL2) | ||
| ENST00000682794.1:n.827dup (BSCL2) | ||
| ENST00000683025.1:c.*164dup (BSCL2) | ENSP00000507028.1:n.*164dup | |
| ENST00000683296.1:c.517dup (BSCL2) | ENSP00000507725.1:p.Thr173AsnfsTer5 | |
| ENST00000683368.1:n.708dup (BSCL2) | ||
| ENST00000683494.1:n.909dup (BSCL2) | ||
| ENST00000683846.1:n.857dup (BSCL2) | ||
| ENST00000683892.1:n.1019dup (BSCL2) | ||
| ENST00000684067.1:c.517dup (BSCL2) | ENSP00000506799.1:p.Thr173AsnfsTer5 | |
| ENST00000684115.1:n.909dup (BSCL2) | ||
| ENST00000684258.1:n.945dup (BSCL2) | ||
| ENST00000684285.1:c.*24dup (BSCL2) | ENSP00000507669.1:n.*24dup | |
| ENST00000684475.1:c.517dup (BSCL2) | ENSP00000507429.1:p.Thr173AsnfsTer5 | |
| ENST00000684609.1:n.909dup (BSCL2) | ||
| ENST00000684720.1:n.909dup (BSCL2) | ||
| ENST00000360796.10:c.517dup (BSCL2) MANE Select | ENSP00000354032.5:p.Thr173AsnfsTer5 | |
| ENST00000679883.1:c.517dup (BSCL2) | ENSP00000505838.1:p.Thr173AsnfsTer5 | |
| ENST00000278893.11:c.325dup (BSCL2) | ENSP00000278893.7:p.Thr109AsnfsTer5 | |
| ENST00000301781.10:c.517dup (BSCL2) | ENSP00000301781.5:p.Thr173AsnfsTer5 | |
| ENST00000360796.9:c.517dup (BSCL2) | ENSP00000354032.5:p.Thr173AsnfsTer5 | |
| ENST00000403550.5:c.325dup (BSCL2) | ENSP00000385561.1:p.Thr109AsnfsTer5 | |
| ENST00000403734.2:c.*568dup (HNRNPUL2-BSCL2) | ENSP00000456010.1:n.*568dup | |
| ENST00000405837.5:c.517dup (BSCL2) | ENSP00000385332.1:p.Thr173AsnfsTer5 | |
| ENST00000407022.7:c.325dup (BSCL2) | ENSP00000384080.3:p.Thr109AsnfsTer5 | |
| ENST00000412351.1:n.115dup (BSCL2) | ||
| ENST00000421906.5:c.325dup (BSCL2) | ENSP00000413209.1:p.Thr109AsnfsTer5 | |
| ENST00000448568.6:c.325dup (BSCL2) | ENSP00000413340.2:p.Thr109AsnfsTer5 | |
| ENST00000524862.5:c.517dup (BSCL2) | ENSP00000433888.1:p.Thr173AsnfsTer5 | |
| ENST00000525000.5:c.149dup (BSCL2) | ||
| ENST00000526426.1:n.32dup (BSCL2) | ||
| ENST00000530900.1:n.317dup (BSCL2) | ||
| ENST00000531524.5:c.118dup (BSCL2) | ENSP00000436026.1:p.Thr40AsnfsTer5 | |
| ENST00000532115.5:n.31dup (BSCL2) | ||
| ENST00000537604.5:n.568dup (BSCL2) | ||
| NM_001122955.3:c.517dup (BSCL2) | NP_001116427.1:p.Thr173AsnfsTer5 | |
| NM_001130702.2:c.325dup (BSCL2) | NP_001124174.2:p.Thr109AsnfsTer5 | |
| NM_032667.6:c.325dup (BSCL2) | NP_116056.3:p.Thr109AsnfsTer5 | |
| NR_037946.1:n.3037dup (HNRNPUL2-BSCL2) | ||
| NR_037948.1:n.1119dup (BSCL2) | ||
| NR_037949.1:n.1119dup (BSCL2) | ||
| NM_001122955.4:c.517dup (BSCL2) MANE Select | NP_001116427.1:p.Thr173AsnfsTer5 | |
| NM_001386027.1:c.517dup (BSCL2) | NP_001372956.1:p.Thr173AsnfsTer5 | |
| NM_001386028.1:c.517dup (BSCL2) | NP_001372957.1:p.Thr173AsnfsTer5 |