Revel Score:
ENST00000302118 (MANE Select)
0.126
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55052329A>G , CM000663.2:g.55052329A>G | GRCh38 |
| NC_000001.10:g.55518002A>G , CM000663.1:g.55518002A>G | GRCh37 |
| NC_000001.9:g.55290590A>G | NCBI36 |
| NG_009061.1:g.17783A>G , LRG_275:g.17783A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.575A>G | ENSP00000501161.2:p.Asp192Gly | |
| ENST00000710286.1:c.932A>G | ENSP00000518176.1:p.Asp311Gly | |
| ENST00000673726.1:c.*71A>G | ENSP00000501004.1:n.*71A>G | |
| ENST00000673903.1:c.200A>G | ENSP00000501257.1:p.Asp67Gly | |
| ENST00000302118.5:c.575A>G MANE Select | ENSP00000303208.5:p.Asp192Gly | |
| ENST00000490692.1:n.1396A>G | ||
| NM_174936.3:c.575A>G , LRG_275t1:c.575A>G | NP_777596.2:p.Asp192Gly | |
| NR_110451.1:n.234A>G | ||
| NM_174936.4:c.575A>G MANE Select | NP_777596.2:p.Asp192Gly | |
| NR_110451.2:n.234A>G |