Linked Data
ClinVar Variation Id:
1656412
ClinVar RCV Id:
RCV002168963
dbSNP Id:
rs370808115
ExAC:
X:153760609 G / A
gnomAD v2:
X-153760609-G-A
gnomAD v3:
X-154532394-G-A
gnomAD v4:
X-154532394-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154532394G>A , CM000685.2:g.154532394G>A | GRCh38 |
| NC_000023.10:g.153760609G>A , CM000685.1:g.153760609G>A | GRCh37 |
| NC_000023.9:g.153413803G>A | NCBI36 |
| NG_009015.2:g.20179C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393564.7:c.1356C>T | ENSP00000377194.2:p.Phe452= | |
| ENST00000439227.6:c.1359C>T | ENSP00000395599.2:p.Phe453= | |
| ENST00000696420.1:c.1356C>T | ENSP00000512615.1:p.Phe452= | |
| ENST00000696421.1:c.1356C>T | ENSP00000512616.1:p.Phe452= | |
| ENST00000696422.1:c.1219C>T | ||
| ENST00000696423.1:c.1222C>T | ||
| ENST00000696424.1:c.1208C>T | ENSP00000512619.1:n.1208C>T | |
| ENST00000696425.1:c.*269C>T | ENSP00000512620.1:n.*269C>T | |
| ENST00000696426.1:c.*816C>T | ENSP00000512621.1:n.*816C>T | |
| ENST00000696427.1:c.*316C>T | ENSP00000512622.1:n.*316C>T | |
| ENST00000696428.1:c.*1198C>T | ENSP00000512623.1:n.*1198C>T | |
| ENST00000696429.1:c.1356C>T | ENSP00000512624.1:p.Phe452= | |
| ENST00000696430.1:c.1356C>T | ENSP00000512625.1:p.Phe452= | |
| ENST00000393562.10:c.1356C>T MANE Select | ENSP00000377192.3:p.Phe452= | |
| ENST00000369620.6:c.1494C>T | ENSP00000358633.2:p.Phe498= | |
| ENST00000393562.6:c.1446C>T | ENSP00000377192.2:p.Phe482= | |
| ENST00000393564.6:c.1356C>T | ENSP00000377194.2:p.Phe452= | |
| ENST00000490651.1:n.577C>T | ||
| ENST00000621232.4:c.1356C>T | ENSP00000483686.1:p.Phe452= | |
| NM_000402.4:c.1446C>T | NP_000393.4:p.Phe482= | |
| NM_001042351.2:c.1356C>T | NP_001035810.1:p.Phe452= | |
| XM_005274657.2:c.1449C>T | XP_005274714.1:p.Phe483= | |
| XM_005274658.2:c.1359C>T | XP_005274715.1:p.Phe453= | |
| NM_001360016.2:c.1356C>T MANE Select | NP_001346945.1:p.Phe452= | |
| NM_001042351.3:c.1356C>T | NP_001035810.1:p.Phe452= |