Revel Score:
ENST00000260947 (MANE Select)
0.037
ENST00000449967
0.037
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.214781126A>C , CM000664.2:g.214781126A>C | GRCh38 |
| NC_000002.11:g.215645850A>C , CM000664.1:g.215645850A>C | GRCh37 |
| NC_000002.10:g.215354095A>C | NCBI36 |
| NG_012047.2:g.33579T>G | |
| NG_012047.3:g.33586T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260947.9:c.748T>G MANE Select | ENSP00000260947.4:p.Ser250Ala | |
| ENST00000421162.2:c.215+15935T>G | ENSP00000392245.2:n.215+15935T>G | |
| ENST00000613192.2:c.158+28286T>G | ENSP00000483275.2:n.158+28286T>G | |
| ENST00000613374.5:c.158+28286T>G | ENSP00000484464.1:n.158+28286T>G | |
| ENST00000613706.5:c.748T>G | ENSP00000484976.2:p.Ser250Ala | |
| ENST00000617164.5:c.691T>G | ENSP00000480470.1:p.Ser231Ala | |
| ENST00000619009.5:c.364+11171T>G | ENSP00000482293.1:n.364+11171T>G | |
| ENST00000650978.1:c.590T>G | ||
| ENST00000260947.8:c.748T>G | ENSP00000260947.4:p.Ser250Ala | |
| ENST00000421162.1:c.215+15935T>G | ENSP00000392245.1:n.215+15935T>G | |
| ENST00000455743.5:c.*368T>G | ENSP00000412186.1:n.*368T>G | |
| ENST00000471787.1:n.643T>G | ||
| ENST00000613192.1:c.73+28286T>G | ENSP00000483275.1:n.73+28286T>G | |
| ENST00000613374.4:c.158+28286T>G | ENSP00000484464.1:n.158+28286T>G | |
| ENST00000613706.4:c.215+15935T>G | ENSP00000484976.1:n.215+15935T>G | |
| ENST00000617164.4:c.691T>G | ENSP00000480470.1:p.Ser231Ala | |
| ENST00000619009.4:c.364+11171T>G | ENSP00000482293.1:n.364+11171T>G | |
| ENST00000620057.4:c.364+11171T>G | ENSP00000481988.1:n.364+11171T>G | |
| NM_000465.3:c.748T>G | NP_000456.2:p.Ser250Ala | |
| NM_001282543.1:c.691T>G | NP_001269472.1:p.Ser231Ala | |
| NM_001282545.1:c.215+15935T>G | NP_001269474.1:n.215+15935T>G | |
| NM_001282548.1:c.158+28286T>G | NP_001269477.1:n.158+28286T>G | |
| NM_001282549.1:c.364+11171T>G | NP_001269478.1:n.364+11171T>G | |
| NR_104212.1:n.741T>G | ||
| NR_104215.1:n.684T>G | ||
| NR_104216.1:n.506+11171T>G | ||
| XM_011511567.1:c.694T>G | XP_011509869.1:p.Ser232Ala | |
| XM_011511568.1:c.748T>G | XP_011509870.1:p.Ser250Ala | |
| XM_017004613.1:c.847T>G | XP_016860102.1:p.Ser283Ala | |
| XM_017004614.1:c.847T>G | XP_016860103.1:p.Ser283Ala | |
| XR_002959322.1:n.938T>G | ||
| NM_000465.4:c.748T>G MANE Select | NP_000456.2:p.Ser250Ala | |
| NM_001282543.2:c.691T>G | NP_001269472.1:p.Ser231Ala | |
| NM_001282545.2:c.215+15935T>G | NP_001269474.1:n.215+15935T>G | |
| NM_001282548.2:c.158+28286T>G | NP_001269477.1:n.158+28286T>G | |
| NM_001282549.2:c.364+11171T>G | NP_001269478.1:n.364+11171T>G | |
| NR_104212.2:n.713T>G | ||
| NR_104215.2:n.656T>G | ||
| NR_104216.2:n.478+11171T>G |