Revel Score:
ENST00000344683 (MANE Select)
0.016
ENST00000519480
0.016
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00000553 (AMR)
Exomes Max Group AF
0.00000741 (AMR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.6439029G>C , CM000670.2:g.6439029G>C | GRCh38 |
| NC_000008.10:g.6296550G>C , CM000670.1:g.6296550G>C | GRCh37 |
| NC_000008.9:g.6283958G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000519480.6:c.513G>C | ENSP00000430962.1:p.Arg171Ser | |
| ENST00000685179.1:c.507G>C | ENSP00000510001.1:p.Arg169Ser | |
| ENST00000686750.1:c.513G>C | ENSP00000509053.1:p.Arg171Ser | |
| ENST00000687720.1:c.*461G>C | ENSP00000510728.1:n.*461G>C | |
| ENST00000687874.1:n.528G>C | ||
| ENST00000688099.1:c.*792G>C | ENSP00000509622.1:n.*792G>C | |
| ENST00000688388.1:c.513G>C | ENSP00000510092.1:p.Arg171Ser | |
| ENST00000688452.1:c.*32G>C | ENSP00000510556.1:n.*32G>C | |
| ENST00000688912.1:n.524G>C | ||
| ENST00000689348.1:c.513G>C | ENSP00000509554.1:p.Arg171Ser | |
| ENST00000689633.1:c.513G>C | ENSP00000509054.1:p.Arg171Ser | |
| ENST00000689736.1:c.513G>C | ENSP00000509722.1:p.Arg171Ser | |
| ENST00000690159.1:c.*792G>C | ENSP00000510482.1:n.*792G>C | |
| ENST00000690518.1:c.*253G>C | ENSP00000509135.1:n.*253G>C | |
| ENST00000690682.1:c.*408G>C | ENSP00000509896.1:n.*408G>C | |
| ENST00000690708.1:c.513G>C | ENSP00000510400.1:p.Arg171Ser | |
| ENST00000690826.1:c.513G>C | ENSP00000510536.1:p.Arg171Ser | |
| ENST00000691435.1:c.513G>C | ENSP00000510652.1:p.Arg171Ser | |
| ENST00000691655.1:c.*523G>C | ENSP00000509652.1:n.*523G>C | |
| ENST00000691738.1:n.721G>C | ||
| ENST00000692836.1:c.513G>C | ENSP00000509971.1:p.Arg171Ser | |
| ENST00000692938.1:c.513G>C | ENSP00000509072.1:p.Arg171Ser | |
| ENST00000693231.1:c.*253G>C | ENSP00000510764.1:n.*253G>C | |
| ENST00000344683.10:c.513G>C MANE Select | ENSP00000342924.5:p.Arg171Ser | |
| ENST00000344683.9:c.513G>C | ENSP00000342924.5:p.Arg171Ser | |
| ENST00000519480.5:c.513G>C | ENSP00000430962.1:p.Arg171Ser | |
| ENST00000522905.1:c.436+2867G>C | ENSP00000430768.1:n.436+2867G>C | |
| NM_001172575.1:c.436+2867G>C | NP_001166046.1:n.436+2867G>C | |
| XM_011534755.1:c.513G>C | XP_011533057.1:p.Arg171Ser | |
| XM_011534756.1:c.513G>C | XP_011533058.1:p.Arg171Ser | |
| XM_011534757.1:c.513G>C | XP_011533059.1:p.Arg171Ser | |
| XM_011534758.1:c.513G>C | XP_011533060.1:p.Arg171Ser | |
| XM_011534759.1:c.513G>C | XP_011533061.1:p.Arg171Ser | |
| XM_011534760.1:c.-13G>C | XP_011533062.1:n.-13G>C | |
| NM_001363979.1:c.513G>C | NP_001350908.1:p.Arg171Ser | |
| NM_001363980.1:c.513G>C | NP_001350909.1:p.Arg171Ser | |
| XM_011534755.3:c.513G>C | XP_011533057.1:p.Arg171Ser | |
| XM_011534756.3:c.513G>C | XP_011533058.1:p.Arg171Ser | |
| XM_011534757.3:c.513G>C | XP_011533059.1:p.Arg171Ser | |
| XM_011534758.3:c.513G>C | XP_011533060.1:p.Arg171Ser | |
| XM_011534759.3:c.513G>C | XP_011533061.1:p.Arg171Ser | |
| XM_011534760.2:c.-13G>C | XP_011533062.1:n.-13G>C | |
| XM_017013829.2:c.513G>C | XP_016869318.1:p.Arg171Ser | |
| XM_017013831.2:c.513G>C | XP_016869320.1:p.Arg171Ser | |
| XM_017013832.2:c.513G>C | XP_016869321.1:p.Arg171Ser | |
| XM_017013833.2:c.513G>C | XP_016869322.1:p.Arg171Ser | |
| XR_001745596.2:n.566G>C | ||
| NM_024596.5:c.513G>C MANE Select | NP_078872.3:p.Arg171Ser | |
| NM_001322042.2:c.513G>C | NP_001308971.2:p.Arg171Ser | |
| NM_001363980.2:c.513G>C | NP_001350909.1:p.Arg171Ser | |
| NM_001172574.2:c.513G>C | NP_001166045.2:p.Arg171Ser | |
| NM_001172575.2:c.436+2867G>C | NP_001166046.1:n.436+2867G>C | |
| NM_001322043.2:c.507G>C | NP_001308972.2:p.Arg169Ser | |
| NM_001322045.2:c.411G>C | NP_001308974.2:p.Arg137Ser | |
| NR_136159.2:n.439G>C |