Revel Score:
ENST00000292901
0.607
ENST00000380299
0.607
ENST00000429817
0.607
gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5234193C>G , CM000673.2:g.5234193C>G | GRCh38 |
| NC_000011.9:g.5255423C>G , CM000673.1:g.5255423C>G | GRCh37 |
| NC_000011.8:g.5211999C>G | NCBI36 |
| NG_000007.3:g.63423G>C | |
| NG_063112.2:g.14465G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000643122.1:c.113G>C | ENSP00000494708.1:p.Trp38Ser | |
| ENST00000650601.1:c.113G>C MANE Select | ENSP00000497529.1:p.Trp38Ser | |
| ENST00000292901.7:c.113G>C | ENSP00000292901.3:p.Trp38Ser | |
| ENST00000380299.3:c.113G>C | ENSP00000369654.3:p.Trp38Ser | |
| ENST00000417377.1:c.92+149G>C | ENSP00000414741.1:n.92+149G>C | |
| ENST00000429817.1:c.113G>C | ENSP00000393810.1:p.Trp38Ser | |
| NM_000519.3:c.113G>C | NP_000510.1:p.Trp38Ser | |
| NM_000519.4:c.113G>C MANE Select | NP_000510.1:p.Trp38Ser |