Revel Score:
ENST00000376592
0.673
ENST00000376583
0.673
ENST00000376590 (MANE Select)
0.673
ENST00000376585
0.673
ENST00000418034
0.673
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.0000122 (NFE)
Exomes Max Group AF
0.00001213 (NFE)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11801220G>A , CM000663.2:g.11801220G>A | GRCh38 |
| NC_000001.10:g.11861277G>A , CM000663.1:g.11861277G>A | GRCh37 |
| NC_000001.9:g.11783864G>A | NCBI36 |
| NG_008766.1:g.71G>A | |
| NG_013351.1:g.9884C>T , LRG_726:g.9884C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376486.3:c.416C>T | ENSP00000365669.3:p.Thr139Met | |
| ENST00000376585.6:c.539C>T | ENSP00000365770.1:p.Thr180Met | |
| ENST00000376590.9:c.416C>T MANE Select | ENSP00000365775.3:p.Thr139Met | |
| ENST00000376592.6:c.416C>T | ENSP00000365777.1:p.Thr139Met | |
| ENST00000423400.7:c.536C>T | ENSP00000398908.3:p.Thr179Met | |
| ENST00000641407.1:c.416C>T | ENSP00000493098.1:p.Thr139Met | |
| ENST00000641437.1:n.548C>T | ||
| ENST00000641446.1:c.416C>T | ENSP00000493262.1:p.Thr139Met | |
| ENST00000641721.1:n.473C>T | ||
| ENST00000641747.1:c.237-898C>T | ENSP00000493116.1:n.237-898C>T | |
| ENST00000641759.1:n.551C>T | ||
| ENST00000641805.1:n.699C>T | ||
| ENST00000641909.1:n.826C>T | ||
| ENST00000376583.7:c.539C>T | ENSP00000365767.3:p.Thr180Met | |
| ENST00000376585.5:c.539C>T | ENSP00000365770.1:p.Thr180Met | |
| ENST00000376590.7:c.416C>T | ENSP00000365775.3:p.Thr139Met | |
| ENST00000376592.5:c.416C>T | ENSP00000365777.1:p.Thr139Met | |
| ENST00000418034.1:c.416C>T | ENSP00000405082.1:p.Thr139Met | |
| NM_005957.4:c.416C>T , LRG_726t1:c.416C>T | NP_005948.3:p.Thr139Met | |
| XM_005263458.2:c.539C>T | XP_005263515.1:p.Thr180Met | |
| XM_005263460.3:c.416C>T | XP_005263517.1:p.Thr139Met | |
| XM_005263461.3:c.416C>T | XP_005263518.1:p.Thr139Met | |
| XM_005263462.3:c.416C>T | XP_005263519.1:p.Thr139Met | |
| XM_005263463.2:c.170C>T | XP_005263520.1:p.Thr57Met | |
| XM_011541495.1:c.536C>T | XP_011539797.1:p.Thr179Met | |
| XM_011541496.1:c.539C>T | XP_011539798.1:p.Thr180Met | |
| NM_001330358.1:c.539C>T | NP_001317287.1:p.Thr180Met | |
| XM_005263460.5:c.416C>T | XP_005263517.1:p.Thr139Met | |
| XM_005263462.4:c.416C>T | XP_005263519.1:p.Thr139Met | |
| XM_005263463.4:c.170C>T | XP_005263520.1:p.Thr57Met | |
| XM_011541495.3:c.536C>T | XP_011539797.1:p.Thr179Met | |
| XM_011541496.3:c.539C>T | XP_011539798.1:p.Thr180Met | |
| XM_017001328.2:c.539C>T | XP_016856817.1:p.Thr180Met | |
| XM_024447198.1:c.170C>T | XP_024302966.1:p.Thr57Met | |
| XR_002956640.1:n.1283C>T | ||
| NM_005957.5:c.416C>T MANE Select | NP_005948.3:p.Thr139Met | |
| NM_001330358.2:c.539C>T | NP_001317287.1:p.Thr180Met |