Revel Score:
ENST00000416691
0.124
ENST00000255468
0.124
ENST00000455146 (MANE Select)
0.124
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00964796 (AFR)
Genomes Max Group AF
0.01001181 (AFR)
Exomes Max Group AF
0.00862904 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.39699514A>G , CM000675.2:g.39699514A>G | GRCh38 |
| NC_000013.10:g.40273651A>G , CM000675.1:g.40273651A>G | GRCh37 |
| NC_000013.9:g.39171651A>G | NCBI36 |
| NG_028352.1:g.48888A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000455146.8:c.1180A>G MANE Select | ENSP00000397441.2:p.Asn394Asp | |
| ENST00000356576.8:c.*1017A>G | ENSP00000348983.4:n.*1017A>G | |
| ENST00000416691.5:c.1180A>G | ENSP00000403733.1:p.Asn394Asp | |
| ENST00000455146.7:c.1180A>G | ENSP00000397441.2:p.Asn394Asp | |
| NM_001145079.1:c.1180A>G | NP_001138551.1:p.Asn394Asp | |
| NM_020751.2:c.1180A>G | NP_065802.1:p.Asn394Asp | |
| NR_026745.1:n.1345A>G | ||
| XM_011535168.1:c.1180A>G | XP_011533470.1:p.Asn394Asp | |
| XM_011535169.1:c.1024A>G | XP_011533471.1:p.Asn342Asp | |
| XM_011535170.1:c.1024A>G | XP_011533472.1:p.Asn342Asp | |
| NM_020751.3:c.1180A>G MANE Select | NP_065802.1:p.Asn394Asp | |
| NM_001145079.2:c.1180A>G | NP_001138551.1:p.Asn394Asp |