Revel Score:
ENST00000265631 (MANE Select)
0.832
ENST00000416240
0.832
ENST00000542654
0.832
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00003588 (SAS)
Exomes Max Group AF
0.00003765 (SAS)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.96121733C>T , CM000669.2:g.96121733C>T | GRCh38 |
| NC_000007.13:g.95751045C>T , CM000669.1:g.95751045C>T | GRCh37 |
| NC_000007.12:g.95588981C>T | NCBI36 |
| NG_012247.1:g.205415G>A | |
| NG_012247.2:g.205415G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265631.10:c.1763G>A MANE Select | ENSP00000265631.6:p.Arg588Gln | |
| ENST00000265631.9:c.1763G>A | ENSP00000265631.5:p.Arg588Gln | |
| ENST00000416240.6:c.1766G>A | ENSP00000400101.2:p.Arg589Gln | |
| ENST00000494085.1:n.266G>A | ||
| NM_001160210.1:c.1766G>A | NP_001153682.1:p.Arg589Gln | |
| NM_014251.2:c.1763G>A | NP_055066.1:p.Arg588Gln | |
| NR_027662.1:n.1838G>A | ||
| XM_006715831.2:c.1796G>A | XP_006715894.1:p.Arg599Gln | |
| XM_011515728.1:c.911G>A | XP_011514030.1:p.Arg304Gln | |
| XM_006715831.4:c.1796G>A | XP_006715894.1:p.Arg599Gln | |
| XM_017011663.1:c.1754G>A | XP_016867152.1:p.Arg585Gln | |
| XM_017011664.2:c.911G>A | XP_016867153.1:p.Arg304Gln | |
| XM_017011665.1:c.911G>A | XP_016867154.1:p.Arg304Gln | |
| XR_001744525.2:n.2009G>A | ||
| XR_002956405.1:n.2567G>A | ||
| NM_014251.3:c.1763G>A MANE Select | NP_055066.1:p.Arg588Gln | |
| NR_027662.2:n.1789G>A | ||
| NM_001160210.2:c.1766G>A | NP_001153682.1:p.Arg589Gln |