Linked Data
ClinVar Variation Id:
402220
ClinVar RCV Id:
RCV000454311
dbSNP Id:
rs1060499779
PubMed:
PMID:26539891
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99013791G>A , CM000670.2:g.99013791G>A | GRCh38 |
| NC_000008.10:g.100026019G>A , CM000670.1:g.100026019G>A | GRCh37 |
| NC_000008.9:g.100095195G>A | NCBI36 |
| NG_007098.2:g.5526G>A , LRG_351:g.5526G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000355155.6:c.3G>A | ENSP00000347281.2:p.Met1Ile | |
| ENST00000682145.1:n.72G>A | ||
| ENST00000682153.1:c.3G>A | ENSP00000507923.1:p.Met1Ile | |
| ENST00000682234.1:c.3G>A | ENSP00000508225.1:p.Met1Ile | |
| ENST00000682358.1:n.73G>A | ||
| ENST00000682806.1:n.104G>A | ||
| ENST00000682853.1:n.108G>A | ||
| ENST00000683334.1:c.3G>A | ENSP00000507369.1:p.Met1Ile | |
| ENST00000683486.1:n.69G>A | ||
| ENST00000683619.1:n.106G>A | ||
| ENST00000683869.1:n.84G>A | ||
| ENST00000684269.1:n.104G>A | ||
| ENST00000684308.1:n.69G>A | ||
| ENST00000357162.7:c.3G>A MANE Select | ENSP00000349685.2:p.Met1Ile | |
| ENST00000358544.7:c.3G>A MANE Plus Clinical | ENSP00000351346.2:p.Met1Ile | |
| ENST00000355155.5:c.3G>A | ENSP00000347281.1:p.Met1Ile | |
| ENST00000357162.6:c.3G>A | ENSP00000349685.2:p.Met1Ile | |
| ENST00000358544.6:c.3G>A | ENSP00000351346.2:p.Met1Ile | |
| ENST00000441350.2:c.3G>A | ENSP00000398472.2:p.Met1Ile | |
| ENST00000496144.5:c.3G>A | ENSP00000430900.1:p.Met1Ile | |
| NM_015243.2:c.3G>A , LRG_351t3:c.3G>A | NP_056058.2:p.Met1Ile | |
| NM_017890.4:c.3G>A , LRG_351t1:c.3G>A | NP_060360.3:p.Met1Ile | |
| NM_152564.4:c.3G>A , LRG_351t2:c.3G>A | NP_689777.3:p.Met1Ile | |
| NM_181661.2:c.3G>A , LRG_351t4:c.3G>A | NP_858047.2:p.Met1Ile | |
| NR_047582.1:n.114G>A | ||
| XM_005250800.2:c.3G>A | XP_005250857.1:p.Met1Ile | |
| XM_005250801.3:c.3G>A | XP_005250858.1:p.Met1Ile | |
| XM_006716510.2:c.3G>A | XP_006716573.1:p.Met1Ile | |
| XM_006716511.2:c.3G>A | XP_006716574.1:p.Met1Ile | |
| XM_011516848.1:c.3G>A | XP_011515150.1:p.Met1Ile | |
| XM_011516849.1:c.3G>A | XP_011515151.1:p.Met1Ile | |
| XM_011516853.1:c.3G>A | XP_011515155.1:p.Met1Ile | |
| XM_011516855.1:c.3G>A | XP_011515157.1:p.Met1Ile | |
| XM_011516856.1:c.3G>A | XP_011515158.1:p.Met1Ile | |
| XM_011516857.1:c.3G>A | XP_011515159.1:p.Met1Ile | |
| XM_011516858.1:c.3G>A | XP_011515160.1:p.Met1Ile | |
| XM_011516859.1:c.3G>A | XP_011515161.1:p.Met1Ile | |
| XM_011516860.1:c.3G>A | XP_011515162.1:p.Met1Ile | |
| XM_011516861.1:c.3G>A | XP_011515163.1:p.Met1Ile | |
| XM_011516862.1:c.3G>A | XP_011515164.1:p.Met1Ile | |
| XM_011516863.1:c.3G>A | XP_011515165.1:p.Met1Ile | |
| XM_011516864.1:c.3G>A | XP_011515166.1:p.Met1Ile | |
| XM_011516865.1:c.3G>A | XP_011515167.1:p.Met1Ile | |
| XM_011516866.1:c.3G>A | XP_011515168.1:p.Met1Ile | |
| XR_928301.1:n.106G>A | ||
| XR_928302.1:n.106G>A | ||
| XR_928303.1:n.106G>A | ||
| XR_928304.1:n.106G>A | ||
| XM_005250800.3:c.3G>A | XP_005250857.1:p.Met1Ile | |
| XM_005250801.5:c.3G>A | XP_005250858.1:p.Met1Ile | |
| XM_006716510.3:c.3G>A | XP_006716573.1:p.Met1Ile | |
| XM_011516848.2:c.3G>A | XP_011515150.1:p.Met1Ile | |
| XM_011516849.2:c.3G>A | XP_011515151.1:p.Met1Ile | |
| XM_011516853.2:c.3G>A | XP_011515155.1:p.Met1Ile | |
| XM_011516859.2:c.3G>A | XP_011515161.1:p.Met1Ile | |
| XM_011516866.2:c.3G>A | XP_011515168.1:p.Met1Ile | |
| XM_017013109.1:c.3G>A | XP_016868598.1:p.Met1Ile | |
| XM_024447074.1:c.-1325G>A | XP_024302842.1:n.-1325G>A | |
| XM_024447075.1:c.3G>A | XP_024302843.1:p.Met1Ile | |
| XR_001745481.1:n.106G>A | ||
| XR_001745482.2:n.106G>A | ||
| XR_001745484.2:n.106G>A | ||
| XR_002956601.1:n.106G>A | ||
| XR_002956602.1:n.106G>A | ||
| XR_928302.2:n.106G>A | ||
| NM_015243.3:c.3G>A | NP_056058.2:p.Met1Ile | |
| NM_017890.5:c.3G>A MANE Plus Clinical | NP_060360.3:p.Met1Ile | |
| NM_152564.5:c.3G>A MANE Select | NP_689777.3:p.Met1Ile | |
| NM_181661.3:c.3G>A | NP_858047.2:p.Met1Ile | |
| NR_047582.2:n.106G>A |