Revel Score:
ENST00000379079
0.333
ENST00000332351
0.333
ENST00000530998
0.333
ENST00000452863 (MANE Select)
0.333
ENST00000448076
0.333
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.32392717G>C , CM000673.2:g.32392717G>C | GRCh38 |
| NC_000011.9:g.32414263G>C , CM000673.1:g.32414263G>C | GRCh37 |
| NC_000011.8:g.32370839G>C | NCBI36 |
| NG_009272.1:g.47825C>G , LRG_525:g.47825C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000332351.9:c.1252C>G | ENSP00000331327.5:p.Arg418Gly | |
| ENST00000379077.9:c.*487C>G | ENSP00000368368.5:n.*487C>G | |
| ENST00000379079.8:c.652C>G | ENSP00000368370.2:p.Arg218Gly | |
| ENST00000448076.9:c.1303C>G | ENSP00000413452.5:p.Arg435Gly | |
| ENST00000452863.10:c.1303C>G MANE Select | ENSP00000415516.5:p.Arg435Gly | |
| ENST00000526685.2:n.757C>G | ||
| ENST00000639563.3:c.1252C>G | ENSP00000492269.3:p.Arg418Gly | |
| ENST00000639907.2:n.446C>G | ||
| ENST00000640146.2:c.628C>G | ENSP00000491984.2:p.Arg210Gly | |
| ENST00000650745.1:n.512C>G | ||
| ENST00000650861.1:n.1884C>G | ||
| ENST00000651459.1:c.74C>G | ||
| ENST00000651533.1:n.349C>G | ||
| ENST00000651668.1:n.240C>G | ||
| ENST00000651794.1:n.1146C>G | ||
| ENST00000651819.1:n.228C>G | ||
| ENST00000652579.1:n.563C>G | ||
| ENST00000652724.1:n.493C>G | ||
| ENST00000332351.7:c.1288C>G | ENSP00000331327.3:p.Arg430Gly | |
| ENST00000379077.7:c.*487C>G | ENSP00000368368.3:n.*487C>G | |
| ENST00000379079.6:c.652C>G | ENSP00000368370.2:p.Arg218Gly | |
| ENST00000448076.7:c.1288C>G | ENSP00000413452.3:p.Arg430Gly | |
| ENST00000452863.7:c.1237C>G | ENSP00000415516.3:p.Arg413Gly | |
| ENST00000527882.5:c.321-653C>G | ||
| ENST00000530998.5:c.601C>G | ENSP00000435307.1:p.Arg201Gly | |
| NM_000378.4:c.1237C>G | NP_000369.3:p.Arg413Gly | |
| NM_001198551.1:c.652C>G , LRG_525t2:c.652C>G | NP_001185480.1:p.Arg218Gly | |
| NM_001198552.1:c.601C>G | NP_001185481.1:p.Arg201Gly | |
| NM_024424.3:c.1288C>G | NP_077742.2:p.Arg430Gly | |
| NM_024426.4:c.1288C>G | NP_077744.3:p.Arg430Gly | |
| NM_000378.5:c.1252C>G | NP_000369.4:p.Arg418Gly | |
| NM_024424.4:c.1303C>G | NP_077742.3:p.Arg435Gly | |
| NM_024426.5:c.1303C>G | NP_077744.4:p.Arg435Gly | |
| NM_001367854.1:c.115C>G | NP_001354783.1:p.Arg39Gly | |
| NR_160306.1:n.1635C>G | ||
| NM_000378.6:c.1252C>G | NP_000369.4:p.Arg418Gly | |
| NM_001198552.2:c.601C>G | NP_001185481.1:p.Arg201Gly | |
| NM_024424.5:c.1303C>G | NP_077742.3:p.Arg435Gly | |
| NM_024426.6:c.1303C>G MANE Select | NP_077744.4:p.Arg435Gly |