Revel Score:
ENST00000260947 (MANE Select)
0.076
ENST00000449967
0.076
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00001473 (SAS)
Exomes Max Group AF
0.00001636 (SAS)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214781282C>A , CM000664.2:g.214781282C>A | GRCh38 |
| NC_000002.11:g.215646006C>A , CM000664.1:g.215646006C>A | GRCh37 |
| NC_000002.10:g.215354251C>A | NCBI36 |
| NG_012047.2:g.33423G>T | |
| NG_012047.3:g.33430G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.592G>T MANE Select | ENSP00000260947.4:p.Ala198Ser | |
| ENST00000421162.2:c.215+15779G>T | ENSP00000392245.2:n.215+15779G>T | |
| ENST00000613192.2:c.158+28130G>T | ENSP00000483275.2:n.158+28130G>T | |
| ENST00000613374.5:c.158+28130G>T | ENSP00000484464.1:n.158+28130G>T | |
| ENST00000613706.5:c.592G>T | ENSP00000484976.2:p.Ala198Ser | |
| ENST00000617164.5:c.535G>T | ENSP00000480470.1:p.Ala179Ser | |
| ENST00000619009.5:c.364+11015G>T | ENSP00000482293.1:n.364+11015G>T | |
| ENST00000650978.1:c.434G>T | ||
| ENST00000260947.8:c.592G>T | ENSP00000260947.4:p.Ala198Ser | |
| ENST00000421162.1:c.215+15779G>T | ENSP00000392245.1:n.215+15779G>T | |
| ENST00000455743.5:c.*212G>T | ENSP00000412186.1:n.*212G>T | |
| ENST00000471787.1:n.487G>T | ||
| ENST00000613192.1:c.73+28130G>T | ENSP00000483275.1:n.73+28130G>T | |
| ENST00000613374.4:c.158+28130G>T | ENSP00000484464.1:n.158+28130G>T | |
| ENST00000613706.4:c.215+15779G>T | ENSP00000484976.1:n.215+15779G>T | |
| ENST00000617164.4:c.535G>T | ENSP00000480470.1:p.Ala179Ser | |
| ENST00000619009.4:c.364+11015G>T | ENSP00000482293.1:n.364+11015G>T | |
| ENST00000620057.4:c.364+11015G>T | ENSP00000481988.1:n.364+11015G>T | |
| NM_000465.3:c.592G>T | NP_000456.2:p.Ala198Ser | |
| NM_001282543.1:c.535G>T | NP_001269472.1:p.Ala179Ser | |
| NM_001282545.1:c.215+15779G>T | NP_001269474.1:n.215+15779G>T | |
| NM_001282548.1:c.158+28130G>T | NP_001269477.1:n.158+28130G>T | |
| NM_001282549.1:c.364+11015G>T | NP_001269478.1:n.364+11015G>T | |
| NR_104212.1:n.585G>T | ||
| NR_104215.1:n.528G>T | ||
| NR_104216.1:n.506+11015G>T | ||
| XM_011511567.1:c.538G>T | XP_011509869.1:p.Ala180Ser | |
| XM_011511568.1:c.592G>T | XP_011509870.1:p.Ala198Ser | |
| XM_017004613.1:c.691G>T | XP_016860102.1:p.Ala231Ser | |
| XM_017004614.1:c.691G>T | XP_016860103.1:p.Ala231Ser | |
| XR_002959322.1:n.782G>T | ||
| NM_000465.4:c.592G>T MANE Select | NP_000456.2:p.Ala198Ser | |
| NM_001282543.2:c.535G>T | NP_001269472.1:p.Ala179Ser | |
| NM_001282545.2:c.215+15779G>T | NP_001269474.1:n.215+15779G>T | |
| NM_001282548.2:c.158+28130G>T | NP_001269477.1:n.158+28130G>T | |
| NM_001282549.2:c.364+11015G>T | NP_001269478.1:n.364+11015G>T | |
| NR_104212.2:n.557G>T | ||
| NR_104215.2:n.500G>T | ||
| NR_104216.2:n.478+11015G>T |