Revel Score:
ENST00000039007 (MANE Select)
0.922
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38403703C>A , CM000685.2:g.38403703C>A | GRCh38 |
| NC_000023.10:g.38262956C>A , CM000685.1:g.38262956C>A | GRCh37 |
| NC_000023.9:g.38147900C>A | NCBI36 |
| NG_008471.1:g.56221C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.626C>A MANE Select | ENSP00000039007.4:p.Ala209Glu | |
| ENST00000643344.1:c.*376C>A | ENSP00000496606.1:n.*376C>A | |
| ENST00000039007.4:c.626C>A | ENSP00000039007.4:p.Ala209Glu | |
| ENST00000465127.1:c.172-262418C>A | ENSP00000417050.1:n.172-262418C>A | |
| NM_000531.5:c.626C>A | NP_000522.3:p.Ala209Glu | |
| XM_017029556.1:c.626C>A | XP_016885045.1:p.Ala209Glu | |
| NM_000531.6:c.626C>A MANE Select | NP_000522.3:p.Ala209Glu |