Linked Data
ClinVar Variation Id:
207578
dbSNP Id:
rs773546205
ExAC:
11:6638255 G / A
gnomAD v2:
11-6638255-G-A
gnomAD v3:
11-6617024-G-A
gnomAD v4:
11-6617024-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6617024G>A , CM000673.2:g.6617024G>A | GRCh38 |
| NC_000011.9:g.6638255G>A , CM000673.1:g.6638255G>A | GRCh37 |
| NC_000011.8:g.6594831G>A | NCBI36 |
| NG_008653.1:g.7438C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682424.1:c.524C>T | ENSP00000507321.1:p.Ser175Leu | |
| ENST00000299427.12:c.638C>T MANE Select | ENSP00000299427.6:p.Ser213Leu | |
| ENST00000436873.7:c.312+277C>T | ||
| ENST00000524788.2:n.1797C>T | ||
| ENST00000524903.2:n.1913C>T | ||
| ENST00000528807.2:n.294C>T | ||
| ENST00000530040.2:n.479+335C>T | ||
| ENST00000533371.6:c.-92C>T | ENSP00000437066.1:n.-92C>T | |
| ENST00000534644.6:n.586C>T | ||
| ENST00000642892.1:c.-92C>T | ENSP00000494165.1:n.-92C>T | |
| ENST00000643439.1:c.*378C>T | ENSP00000495849.1:n.*378C>T | |
| ENST00000643479.1:n.667C>T | ||
| ENST00000643516.1:c.395+277C>T | ||
| ENST00000644151.1:n.2077C>T | ||
| ENST00000644218.1:c.638C>T | ENSP00000493574.1:p.Ser213Leu | |
| ENST00000644683.1:c.*91C>T | ENSP00000494085.1:n.*91C>T | |
| ENST00000644810.1:c.359C>T | ENSP00000495895.1:p.Ser120Leu | |
| ENST00000644831.1:n.814C>T | ||
| ENST00000644933.1:c.-92C>T | ENSP00000496133.1:n.-92C>T | |
| ENST00000645020.1:n.1813C>T | ||
| ENST00000645285.1:c.-92C>T | ENSP00000495058.1:n.-92C>T | |
| ENST00000645331.1:n.1004C>T | ||
| ENST00000645620.1:c.-92C>T | ENSP00000493657.1:n.-92C>T | |
| ENST00000646777.1:n.814C>T | ||
| ENST00000647016.1:n.1118C>T | ||
| ENST00000647152.1:c.-92C>T | ENSP00000495893.1:n.-92C>T | |
| ENST00000647209.1:c.*507C>T | ENSP00000495558.1:n.*507C>T | |
| ENST00000647346.1:n.1658C>T | ||
| ENST00000299427.10:c.638C>T | ENSP00000299427.6:p.Ser213Leu | |
| ENST00000428886.6:n.807C>T | ||
| ENST00000436873.6:c.450+335C>T | ENSP00000398136.2:n.450+335C>T | |
| ENST00000524788.1:n.338C>T | ||
| ENST00000528571.5:c.*378C>T | ENSP00000434647.1:n.*378C>T | |
| ENST00000528807.1:n.188C>T | ||
| ENST00000533371.5:c.-92C>T | ENSP00000437066.1:n.-92C>T | |
| ENST00000534644.5:n.623C>T | ||
| ENST00000611494.4:c.638C>T | ENSP00000484546.1:p.Ser213Leu | |
| NM_000391.3:c.638C>T | NP_000382.3:p.Ser213Leu | |
| NM_000391.4:c.638C>T MANE Select | NP_000382.3:p.Ser213Leu |