Linked Data
ClinVar Variation Id:
653111
dbSNP Id:
rs371316167
ExAC:
17:7127641 C / T
gnomAD v2:
17-7127641-C-T
gnomAD v3:
17-7224322-C-T
gnomAD v4:
17-7224322-C-T
COSMIC:
COSM5972387
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224322C>T , CM000679.2:g.7224322C>T | GRCh38 |
| NC_000017.10:g.7127641C>T , CM000679.1:g.7127641C>T | GRCh37 |
| NC_000017.9:g.7068365C>T | NCBI36 |
| NG_007975.1:g.9489C>T | |
| NG_008391.2:g.729G>A | |
| NG_033038.1:g.15223G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1534C>T MANE Select | ENSP00000349297.5:p.Arg512Trp | |
| ENST00000322910.9:c.*1489C>T | ENSP00000325395.5:n.*1489C>T | |
| ENST00000350303.9:c.1468C>T | ENSP00000344152.5:p.Arg490Trp | |
| ENST00000356839.9:c.1534C>T | ENSP00000349297.5:p.Arg512Trp | |
| ENST00000542255.6:c.392C>T | ||
| ENST00000543245.6:c.1603C>T | ENSP00000438689.2:p.Arg535Trp | |
| ENST00000578319.5:n.29C>T | ||
| ENST00000578711.1:n.818C>T | ||
| ENST00000578809.5:n.106C>T | ||
| ENST00000579391.1:n.142C>T | ||
| ENST00000579425.5:n.650C>T | ||
| ENST00000579546.1:c.273C>T | ||
| ENST00000579894.5:n.321C>T | ||
| ENST00000582450.1:n.42C>T | ||
| ENST00000583074.5:n.155C>T | ||
| ENST00000583850.5:n.309C>T | ||
| ENST00000583858.5:c.465C>T | ||
| ENST00000585203.6:n.725C>T | ||
| NM_000018.3:c.1534C>T | NP_000009.1:p.Arg512Trp | |
| NM_001033859.2:c.1468C>T | NP_001029031.1:p.Arg490Trp | |
| NM_001270447.1:c.1603C>T | NP_001257376.1:p.Arg535Trp | |
| NM_001270448.1:c.1306C>T | NP_001257377.1:p.Arg436Trp | |
| XM_006721516.2:c.1534C>T | XP_006721579.2:p.Arg512Trp | |
| XM_011523829.1:c.1436C>T | XP_011522131.1:p.Ala479Val | |
| XM_011523830.1:c.1436C>T | XP_011522132.1:p.Ala479Val | |
| XR_934021.1:n.1641C>T | ||
| XR_934022.1:n.1543C>T | ||
| XR_934023.1:n.1543C>T | ||
| XM_006721516.3:c.1534C>T | XP_006721579.2:p.Arg512Trp | |
| XM_011523829.2:c.1436C>T | XP_011522131.1:p.Ala479Val | |
| XM_011523830.2:c.1436C>T | XP_011522132.1:p.Ala479Val | |
| XM_024450741.1:c.1436C>T | XP_024306509.1:p.Ala479Val | |
| XR_934021.2:n.1593C>T | ||
| XR_934022.2:n.1495C>T | ||
| XR_934023.2:n.1495C>T | ||
| NM_000018.4:c.1534C>T MANE Select | NP_000009.1:p.Arg512Trp | |
| NM_001033859.3:c.1468C>T | NP_001029031.1:p.Arg490Trp | |
| NM_001270447.2:c.1603C>T | NP_001257376.1:p.Arg535Trp | |
| NM_001270448.2:c.1306C>T | NP_001257377.1:p.Arg436Trp |