Revel Score:
ENST00000262418 (MANE Select)
0.138
gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44251253G>T , CM000679.2:g.44251253G>T | GRCh38 |
| NC_000017.10:g.42328621G>T , CM000679.1:g.42328621G>T | GRCh37 |
| NC_000017.9:g.39684147G>T | NCBI36 |
| NG_007498.1:g.21882C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262418.12:c.2561C>A MANE Select | ENSP00000262418.6:p.Pro854Gln | |
| ENST00000262418.10:c.2561C>A | ENSP00000262418.6:p.Pro854Gln | |
| ENST00000399246.3:c.1463C>A | ENSP00000382190.3:p.Pro488Gln | |
| NM_000342.3:c.2561C>A | NP_000333.1:p.Pro854Gln | |
| XM_005257593.3:c.2366C>A | XP_005257650.1:p.Pro789Gln | |
| XM_011525129.1:c.2471C>A | XP_011523431.1:p.Pro824Gln | |
| XM_005257593.5:c.2366C>A | XP_005257650.1:p.Pro789Gln | |
| XM_011525129.2:c.2471C>A | XP_011523431.1:p.Pro824Gln | |
| NM_000342.4:c.2561C>A MANE Select | NP_000333.1:p.Pro854Gln |