Linked Data
gnomAD v4:
17-8232098-G-A
COSMIC:
COSM986237
MyVariant Identifiers:
chr17:g.8135416G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8232098G>A , CM000679.2:g.8232098G>A | GRCh38 |
| NC_000017.10:g.8135416G>A , CM000679.1:g.8135416G>A | GRCh37 |
| NC_000017.9:g.8076141G>A | NCBI36 |
| NG_032148.1:g.20998C>T | |
| NG_032148.2:g.20998C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000580299.2:c.2190C>T | ENSP00000462607.2:p.Ser730= | |
| ENST00000581729.2:c.2190C>T | ENSP00000462720.2:p.Ser730= | |
| ENST00000581967.2:n.2642C>T | ||
| ENST00000583254.2:n.2896C>T | ||
| ENST00000699849.1:c.1293C>T | ENSP00000514647.1:p.Ser431= | |
| ENST00000699850.1:n.1453C>T | ||
| ENST00000699851.1:n.2212C>T | ||
| ENST00000699852.1:c.*866C>T | ENSP00000514648.1:n.*866C>T | |
| ENST00000699853.1:c.2190C>T | ENSP00000514649.1:p.Ser730= | |
| ENST00000699854.1:n.1983C>T | ||
| ENST00000699855.1:n.2642C>T | ||
| ENST00000699856.1:c.2190C>T | ENSP00000514650.1:p.Ser730= | |
| ENST00000699857.1:n.2198C>T | ||
| ENST00000699858.1:c.*803C>T | ENSP00000514651.1:n.*803C>T | |
| ENST00000699859.1:c.2061C>T | ENSP00000514652.1:p.Ser687= | |
| ENST00000699860.1:n.296C>T | ||
| ENST00000699861.1:n.2212C>T | ||
| ENST00000699862.1:n.3150C>T | ||
| ENST00000449476.7:c.2085C>T | ENSP00000396018.2:p.Ser695= | |
| ENST00000581671.2:n.2179C>T | ||
| ENST00000643543.1:c.*897C>T | ENSP00000494323.1:n.*897C>T | |
| ENST00000651323.1:c.2190C>T MANE Select | ENSP00000498499.1:p.Ser730= | |
| ENST00000315684.12:c.2190C>T | ENSP00000313759.8:p.Ser730= | |
| ENST00000449476.6:c.2085C>T | ENSP00000396018.2:p.Ser695= | |
| ENST00000578240.1:n.418C>T | ||
| ENST00000578537.1:c.86C>T | ||
| NM_025099.5:c.2190C>T | NP_079375.3:p.Ser730= | |
| NR_046431.1:n.2144C>T | ||
| XM_006721577.2:c.2061C>T | XP_006721640.1:p.Ser687= | |
| XM_006721578.2:c.2190C>T | XP_006721641.1:p.Ser730= | |
| XM_006721579.2:c.2190C>T | XP_006721642.1:p.Ser730= | |
| XM_011524010.1:c.2085C>T | XP_011522312.1:p.Ser695= | |
| XM_011524011.1:c.1293C>T | XP_011522313.1:p.Ser431= | |
| XR_429823.2:n.2233C>T | ||
| XR_429824.2:n.2233C>T | ||
| XR_429825.1:n.2233C>T | ||
| NM_025099.6:c.2190C>T MANE Select | NP_079375.3:p.Ser730= | |
| XM_006721577.3:c.2061C>T | XP_006721640.1:p.Ser687= | |
| XM_006721578.3:c.2190C>T | XP_006721641.1:p.Ser730= | |
| XM_011524010.2:c.2085C>T | XP_011522312.1:p.Ser695= | |
| XM_011524011.2:c.1293C>T | XP_011522313.1:p.Ser431= | |
| XR_001752639.1:n.2104C>T | ||
| XR_001752640.1:n.2233C>T | ||
| XR_001752641.1:n.2233C>T | ||
| XR_001752642.1:n.2233C>T | ||
| XR_001752643.1:n.2663C>T | ||
| XR_002958073.1:n.2233C>T | ||
| XR_429823.3:n.2233C>T | ||
| XR_429824.3:n.2233C>T | ||
| NR_046431.2:n.2105C>T |