Revel Score:
ENST00000446804
0.050
ENST00000311907 (MANE Select)
0.107
ENST00000530231
0.107
ENST00000442468
0.107
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46723453C>G , CM000673.2:g.46723453C>G | GRCh38 |
| NC_000011.9:g.46745003C>G , CM000673.1:g.46745003C>G | GRCh37 |
| NC_000011.8:g.46701579C>G | NCBI36 |
| NG_008953.1:g.9261C>G , LRG_551:g.9261C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311907.10:c.494C>G MANE Select | ENSP00000308541.5:p.Thr165Arg | |
| ENST00000311907.9:c.494C>G | ENSP00000308541.5:p.Thr165Arg | |
| ENST00000442468.1:c.464C>G | ENSP00000387413.1:p.Thr155Arg | |
| ENST00000490274.1:n.274C>G | ||
| ENST00000530231.5:c.494C>G | ENSP00000433907.1:p.Thr165Arg | |
| NM_000506.3:c.494C>G | NP_000497.1:p.Thr165Arg | |
| NM_000506.4:c.494C>G , LRG_551t1:c.494C>G | NP_000497.1:p.Thr165Arg | |
| NM_001311257.1:c.446C>G | NP_001298186.1:p.Thr149Arg | |
| XR_428840.2:n.538C>G | ||
| XR_428840.4:n.529C>G | ||
| NM_000506.5:c.494C>G MANE Select | NP_000497.1:p.Thr165Arg | |
| NM_001311257.2:c.446C>G | NP_001298186.1:p.Thr149Arg |