Linked Data
ClinVar Variation Id:
543290
dbSNP Id:
rs746737457
ExAC:
11:62458311 C / T
gnomAD v2:
11-62458311-C-T
gnomAD v3:
11-62690839-C-T
gnomAD v4:
11-62690839-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.62690839C>T , CM000673.2:g.62690839C>T | GRCh38 |
| NC_000011.9:g.62458311C>T , CM000673.1:g.62458311C>T | GRCh37 |
| NC_000011.8:g.62214887C>T | NCBI36 |
| NG_008461.1:g.23736G>A | |
| NG_033077.1:g.4061G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000412351.2:n.1431G>A (BSCL2) | ||
| ENST00000449636.6:c.609G>A (BSCL2) | ENSP00000405265.2:p.Pro203= | |
| ENST00000463679.6:n.1091G>A (BSCL2) | ||
| ENST00000524862.6:c.1101G>A (BSCL2) | ENSP00000433888.2:p.Pro367= | |
| ENST00000682003.1:n.1489G>A (BSCL2) | ||
| ENST00000682223.1:c.1101G>A (BSCL2) | ENSP00000508140.1:p.Pro367= | |
| ENST00000682262.1:c.*163G>A (BSCL2) | ENSP00000507103.1:n.*163G>A | |
| ENST00000682555.1:c.*212G>A (BSCL2) | ENSP00000507814.1:n.*212G>A | |
| ENST00000682644.1:n.1838G>A (BSCL2) | ||
| ENST00000682794.1:n.1618G>A (BSCL2) | ||
| ENST00000683025.1:c.*886G>A (BSCL2) | ENSP00000507028.1:n.*886G>A | |
| ENST00000683193.1:n.821G>A (BSCL2) | ||
| ENST00000683296.1:c.1101G>A (BSCL2) | ENSP00000507725.1:p.Pro367= | |
| ENST00000683368.1:n.1499G>A (BSCL2) | ||
| ENST00000683494.1:n.2981G>A (BSCL2) | ||
| ENST00000683846.1:n.1441G>A (BSCL2) | ||
| ENST00000683892.1:n.1741G>A (BSCL2) | ||
| ENST00000684067.1:c.1073-108G>A (BSCL2) | ENSP00000506799.1:n.1073-108G>A | |
| ENST00000684115.1:n.1682G>A (BSCL2) | ||
| ENST00000684258.1:n.1874G>A (BSCL2) | ||
| ENST00000684285.1:c.*608G>A (BSCL2) | ENSP00000507669.1:n.*608G>A | |
| ENST00000684475.1:c.966G>A (BSCL2) | ENSP00000507429.1:p.Pro322= | |
| ENST00000684609.1:n.1838G>A (BSCL2) | ||
| ENST00000684720.1:n.2792G>A (BSCL2) | ||
| ENST00000360796.10:c.1101G>A (BSCL2) MANE Select | ENSP00000354032.5:p.Pro367= | |
| ENST00000679883.1:c.1101G>A (BSCL2) | ENSP00000505838.1:p.Pro367= | |
| ENST00000278893.11:c.767G>A (BSCL2) | ENSP00000278893.7:p.Arg256His | |
| ENST00000301781.10:c.*212G>A (BSCL2) | ENSP00000301781.5:n.*212G>A | |
| ENST00000360796.9:c.1101G>A (BSCL2) | ENSP00000354032.5:p.Pro367= | |
| ENST00000403098.6:c.186-418G>A (BSCL2) | ENSP00000384258.2:n.186-418G>A | |
| ENST00000403550.5:c.909G>A (BSCL2) | ENSP00000385561.1:p.Pro303= | |
| ENST00000403734.2:c.*1152G>A (HNRNPUL2-BSCL2) | ENSP00000456010.1:n.*1152G>A | |
| ENST00000405837.5:c.1107G>A (BSCL2) | ENSP00000385332.1:p.Pro369= | |
| ENST00000407022.7:c.909G>A (BSCL2) | ENSP00000384080.3:p.Pro303= | |
| ENST00000421906.5:c.909G>A (BSCL2) | ENSP00000413209.1:p.Pro303= | |
| ENST00000449636.5:c.156G>A (BSCL2) | ENSP00000405265.1:p.Pro52= | |
| ENST00000463679.5:n.504G>A (BSCL2) | ||
| ENST00000470529.5:n.133G>A (BSCL2) | ||
| NM_001122955.3:c.1101G>A (BSCL2) | NP_001116427.1:p.Pro367= | |
| NM_001130702.2:c.767G>A (BSCL2) | NP_001124174.2:p.Arg256His | |
| NM_032667.6:c.909G>A (BSCL2) | NP_116056.3:p.Pro303= | |
| NR_037946.1:n.3621G>A (HNRNPUL2-BSCL2) | ||
| NR_037948.1:n.1703G>A (BSCL2) | ||
| NR_037949.1:n.1709G>A (BSCL2) | ||
| NM_001122955.4:c.1101G>A (BSCL2) MANE Select | NP_001116427.1:p.Pro367= | |
| NM_001386027.1:c.1107G>A (BSCL2) | NP_001372956.1:p.Pro369= | |
| NM_001386028.1:c.1101G>A (BSCL2) | NP_001372957.1:p.Pro367= |