Revel Score:
ENST00000260947 (MANE Select)
0.055
ENST00000449967
0.055
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214780967C>T , CM000664.2:g.214780967C>T | GRCh38 |
| NC_000002.11:g.215645691C>T , CM000664.1:g.215645691C>T | GRCh37 |
| NC_000002.10:g.215353936C>T | NCBI36 |
| NG_012047.2:g.33738G>A | |
| NG_012047.3:g.33745G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.907G>A MANE Select | ENSP00000260947.4:p.Val303Ile | |
| ENST00000421162.2:c.215+16094G>A | ENSP00000392245.2:n.215+16094G>A | |
| ENST00000613192.2:c.158+28445G>A | ENSP00000483275.2:n.158+28445G>A | |
| ENST00000613374.5:c.159-28412G>A | ENSP00000484464.1:n.159-28412G>A | |
| ENST00000613706.5:c.906+1G>A | ENSP00000484976.2:n.906+1G>A | |
| ENST00000617164.5:c.850G>A | ENSP00000480470.1:p.Val284Ile | |
| ENST00000619009.5:c.364+11330G>A | ENSP00000482293.1:n.364+11330G>A | |
| ENST00000650978.1:c.749G>A | ||
| ENST00000260947.8:c.907G>A | ENSP00000260947.4:p.Val303Ile | |
| ENST00000421162.1:c.215+16094G>A | ENSP00000392245.1:n.215+16094G>A | |
| ENST00000455743.5:c.*527G>A | ENSP00000412186.1:n.*527G>A | |
| ENST00000471787.1:n.802G>A | ||
| ENST00000613192.1:c.73+28445G>A | ENSP00000483275.1:n.73+28445G>A | |
| ENST00000613374.4:c.159-28412G>A | ENSP00000484464.1:n.159-28412G>A | |
| ENST00000613706.4:c.215+16094G>A | ENSP00000484976.1:n.215+16094G>A | |
| ENST00000617164.4:c.850G>A | ENSP00000480470.1:p.Val284Ile | |
| ENST00000619009.4:c.364+11330G>A | ENSP00000482293.1:n.364+11330G>A | |
| ENST00000620057.4:c.364+11330G>A | ENSP00000481988.1:n.364+11330G>A | |
| NM_000465.3:c.907G>A | NP_000456.2:p.Val303Ile | |
| NM_001282543.1:c.850G>A | NP_001269472.1:p.Val284Ile | |
| NM_001282545.1:c.215+16094G>A | NP_001269474.1:n.215+16094G>A | |
| NM_001282548.1:c.159-28412G>A | NP_001269477.1:n.159-28412G>A | |
| NM_001282549.1:c.364+11330G>A | NP_001269478.1:n.364+11330G>A | |
| NR_104212.1:n.900G>A | ||
| NR_104215.1:n.843G>A | ||
| NR_104216.1:n.506+11330G>A | ||
| XM_011511567.1:c.853G>A | XP_011509869.1:p.Val285Ile | |
| XM_011511568.1:c.907G>A | XP_011509870.1:p.Val303Ile | |
| XM_017004613.1:c.1006G>A | XP_016860102.1:p.Val336Ile | |
| XM_017004614.1:c.1006G>A | XP_016860103.1:p.Val336Ile | |
| XR_002959322.1:n.1097G>A | ||
| NM_000465.4:c.907G>A MANE Select | NP_000456.2:p.Val303Ile | |
| NM_001282543.2:c.850G>A | NP_001269472.1:p.Val284Ile | |
| NM_001282545.2:c.215+16094G>A | NP_001269474.1:n.215+16094G>A | |
| NM_001282548.2:c.159-28412G>A | NP_001269477.1:n.159-28412G>A | |
| NM_001282549.2:c.364+11330G>A | NP_001269478.1:n.364+11330G>A | |
| NR_104212.2:n.872G>A | ||
| NR_104215.2:n.815G>A | ||
| NR_104216.2:n.478+11330G>A |