Revel Score:
ENST00000277541
0.622
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136517851G>C , CM000671.2:g.136517851G>C | GRCh38 |
| NC_000009.11:g.139412303G>C , CM000671.1:g.139412303G>C | GRCh37 |
| NC_000009.10:g.138532124G>C | NCBI36 |
| NG_007458.1:g.32936C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651671.1:c.1342C>G MANE Select | ENSP00000498587.1:p.Arg448Gly | |
| ENST00000679595.1:c.1342C>G | ENSP00000506241.1:p.Arg448Gly | |
| ENST00000680133.1:c.1342C>G | ENSP00000505319.1:p.Arg448Gly | |
| ENST00000680218.1:c.1342C>G | ENSP00000505339.1:p.Arg448Gly | |
| ENST00000680668.1:c.1342C>G | ENSP00000506336.1:p.Arg448Gly | |
| ENST00000680924.1:c.1342C>G | ENSP00000506031.1:p.Arg448Gly | |
| ENST00000681135.1:c.1342C>G | ENSP00000506636.1:p.Arg448Gly | |
| ENST00000681454.1:c.*578C>G | ENSP00000505763.1:n.*578C>G | |
| ENST00000277541.6:c.1342C>G | ENSP00000277541.6:p.Arg448Gly | |
| NM_017617.3:c.1342C>G | NP_060087.3:p.Arg448Gly | |
| XM_011518717.1:c.643C>G | XP_011517019.1:p.Arg215Gly | |
| NM_017617.5:c.1342C>G MANE Select | NP_060087.3:p.Arg448Gly | |
| XM_011518717.2:c.619C>G | XP_011517019.2:p.Arg207Gly |