Revel Score:
ENST00000375244
0.643
ENST00000375247
0.643
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.32081419C>G , CM000668.2:g.32081419C>G | GRCh38 |
| NC_000006.11:g.32049196C>G , CM000668.1:g.32049196C>G | GRCh37 |
| NC_000006.10:g.32157174C>G | NCBI36 |
| NG_008337.2:g.32956G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644971.2:c.3991G>C MANE Select | ENSP00000496448.1:p.Gly1331Arg | |
| ENST00000647633.1:c.4732G>C | ENSP00000497649.1:p.Gly1578Arg | |
| ENST00000375244.7:c.3991G>C | ENSP00000364393.3:p.Gly1331Arg | |
| ENST00000613214.4:c.4252G>C | ENSP00000480067.1:p.Gly1418Arg | |
| NM_019105.6:c.3991G>C | NP_061978.6:p.Gly1331Arg | |
| NM_001365276.1:c.3991G>C | NP_001352205.1:p.Gly1331Arg | |
| NM_019105.7:c.3991G>C | NP_061978.6:p.Gly1331Arg | |
| NM_001365276.2:c.3991G>C MANE Select | NP_001352205.1:p.Gly1331Arg | |
| NM_019105.8:c.3991G>C | NP_061978.6:p.Gly1331Arg |