Linked Data
ClinVar Variation Id:
861088
ClinVar RCV Id:
RCV001067527
dbSNP Id:
rs758840412
ExAC:
8:100403838 T / A
gnomAD v2:
8-100403838-T-A
gnomAD v4:
8-99391610-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.99391610T>A , CM000670.2:g.99391610T>A | GRCh38 |
| NC_000008.10:g.100403838T>A , CM000670.1:g.100403838T>A | GRCh37 |
| NC_000008.9:g.100473014T>A | NCBI36 |
| NG_007098.2:g.383345T>A , LRG_351:g.383345T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355155.6:c.2985T>A | ENSP00000347281.2:p.Asp995Glu | |
| ENST00000682145.1:n.2865T>A | ||
| ENST00000682153.1:c.2988T>A | ENSP00000507923.1:p.Asp996Glu | |
| ENST00000682234.1:c.2988T>A | ENSP00000508225.1:p.Asp996Glu | |
| ENST00000682358.1:n.3058T>A | ||
| ENST00000683334.1:c.2988T>A | ENSP00000507369.1:p.Asp996Glu | |
| ENST00000683486.1:n.3054T>A | ||
| ENST00000683619.1:n.3160T>A | ||
| ENST00000683869.1:n.3069T>A | ||
| ENST00000357162.7:c.2988T>A MANE Select | ENSP00000349685.2:p.Asp996Glu | |
| ENST00000358544.7:c.2988T>A MANE Plus Clinical | ENSP00000351346.2:p.Asp996Glu | |
| ENST00000357162.6:c.2988T>A | ENSP00000349685.2:p.Asp996Glu | |
| ENST00000358544.6:c.2988T>A | ENSP00000351346.2:p.Asp996Glu | |
| ENST00000496144.5:c.2988T>A | ENSP00000430900.1:p.Asp996Glu | |
| ENST00000521037.1:n.159T>A | ||
| ENST00000522802.5:n.210T>A | ||
| NM_017890.4:c.2988T>A , LRG_351t1:c.2988T>A | NP_060360.3:p.Asp996Glu | |
| NM_152564.4:c.2988T>A , LRG_351t2:c.2988T>A | NP_689777.3:p.Asp996Glu | |
| XM_005250800.2:c.2988T>A | XP_005250857.1:p.Asp996Glu | |
| XM_005250801.3:c.2988T>A | XP_005250858.1:p.Asp996Glu | |
| XM_006716510.2:c.2988T>A | XP_006716573.1:p.Asp996Glu | |
| XM_011516848.1:c.2985T>A | XP_011515150.1:p.Asp995Glu | |
| XM_011516849.1:c.2988T>A | XP_011515151.1:p.Asp996Glu | |
| XM_011516850.1:c.2610T>A | XP_011515152.1:p.Asp870Glu | |
| XM_011516853.1:c.2988T>A | XP_011515155.1:p.Asp996Glu | |
| XM_011516855.1:c.2988T>A | XP_011515157.1:p.Asp996Glu | |
| XM_011516856.1:c.2988T>A | XP_011515158.1:p.Asp996Glu | |
| XM_011516857.1:c.2988T>A | XP_011515159.1:p.Asp996Glu | |
| XM_011516858.1:c.2988T>A | XP_011515160.1:p.Asp996Glu | |
| XM_011516859.1:c.2988T>A | XP_011515161.1:p.Asp996Glu | |
| XM_011516860.1:c.2988T>A | XP_011515162.1:p.Asp996Glu | |
| XM_011516861.1:c.2988T>A | XP_011515163.1:p.Asp996Glu | |
| XR_928301.1:n.3091T>A | ||
| XR_928302.1:n.3091T>A | ||
| XR_928303.1:n.3091T>A | ||
| XR_928304.1:n.3091T>A | ||
| XM_005250800.3:c.2988T>A | XP_005250857.1:p.Asp996Glu | |
| XM_005250801.5:c.2988T>A | XP_005250858.1:p.Asp996Glu | |
| XM_006716510.3:c.2988T>A | XP_006716573.1:p.Asp996Glu | |
| XM_011516848.2:c.2985T>A | XP_011515150.1:p.Asp995Glu | |
| XM_011516849.2:c.2988T>A | XP_011515151.1:p.Asp996Glu | |
| XM_011516850.2:c.2610T>A | XP_011515152.1:p.Asp870Glu | |
| XM_011516853.2:c.2988T>A | XP_011515155.1:p.Asp996Glu | |
| XM_011516859.2:c.2988T>A | XP_011515161.1:p.Asp996Glu | |
| XM_017013109.1:c.2793T>A | XP_016868598.1:p.Asp931Glu | |
| XM_024447074.1:c.1773T>A | XP_024302842.1:p.Asp591Glu | |
| XM_024447075.1:c.2988T>A | XP_024302843.1:p.Asp996Glu | |
| XR_001745481.1:n.3091T>A | ||
| XR_001745482.2:n.3091T>A | ||
| XR_001745484.2:n.3091T>A | ||
| XR_002956601.1:n.3088T>A | ||
| XR_002956602.1:n.3091T>A | ||
| XR_928302.2:n.3091T>A | ||
| NM_017890.5:c.2988T>A MANE Plus Clinical | NP_060360.3:p.Asp996Glu | |
| NM_152564.5:c.2988T>A MANE Select | NP_689777.3:p.Asp996Glu |