Revel Score:
ENST00000260630
0.104
ENST00000407341
0.104
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38070855G>C , CM000664.2:g.38070855G>C | GRCh38 |
| NC_000002.11:g.38297998G>C , CM000664.1:g.38297998G>C | GRCh37 |
| NC_000002.10:g.38151502G>C | NCBI36 |
| NG_008386.2:g.10247C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000490576.2:c.1499C>G | ENSP00000478839.2:p.Pro500Arg | |
| ENST00000610745.5:c.1499C>G MANE Select | ENSP00000478561.1:p.Pro500Arg | |
| ENST00000494864.1:c.386C>G | ENSP00000479876.1:p.Pro129Arg | |
| ENST00000610745.4:c.1499C>G | ENSP00000478561.1:p.Pro500Arg | |
| ENST00000614273.1:c.1499C>G | ENSP00000483678.1:p.Pro500Arg | |
| NM_000104.3:c.1499C>G | NP_000095.2:p.Pro500Arg | |
| NM_000104.4:c.1499C>G MANE Select | NP_000095.2:p.Pro500Arg |