Revel Score:
ENST00000262648 (MANE Select)
0.352
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.8536852C>T , CM000685.2:g.8536852C>T | GRCh38 |
| NC_000023.10:g.8504893C>T , CM000685.1:g.8504893C>T | GRCh37 |
| NC_000023.9:g.8464893C>T | NCBI36 |
| NG_007088.1:g.200335G>A | |
| NG_007088.2:g.200335G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262648.8:c.1540G>A MANE Select | ENSP00000262648.3:p.Glu514Lys | |
| ENST00000262648.7:c.1540G>A | ENSP00000262648.3:p.Glu514Lys | |
| ENST00000481896.1:n.85G>A | ||
| ENST00000619786.1:c.1537G>A | ENSP00000478734.1:p.Glu513Lys | |
| NM_000216.2:c.1540G>A | NP_000207.2:p.Glu514Lys | |
| NM_000216.3:c.1540G>A | NP_000207.2:p.Glu514Lys | |
| NM_000216.4:c.1540G>A MANE Select | NP_000207.2:p.Glu514Lys |