Revel Score:
ENST00000541158
0.505
ENST00000412429
0.505
ENST00000298171 (MANE Select)
0.505
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.81143951C>A , CM000676.2:g.81143951C>A | GRCh38 |
| NC_000014.8:g.81610295C>A , CM000676.1:g.81610295C>A | GRCh37 |
| NC_000014.7:g.80680048C>A | NCBI36 |
| NG_009206.1:g.193427C>A , LRG_523:g.193427C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298171.7:c.1893C>A MANE Select | ENSP00000298171.2:p.Phe631Leu | |
| ENST00000637447.1:c.796C>A | ||
| ENST00000298171.6:c.1893C>A | ENSP00000298171.2:p.Phe631Leu | |
| ENST00000541158.6:c.1893C>A | ENSP00000441235.2:p.Phe631Leu | |
| NM_000369.2:c.1893C>A , LRG_523t1:c.1893C>A | NP_000360.2:p.Phe631Leu | |
| XM_005268037.3:c.1893C>A | XP_005268094.1:p.Phe631Leu | |
| XM_011537119.1:c.1614C>A | XP_011535421.1:p.Phe538Leu | |
| XR_245790.3:n.2086+21242G>T | ||
| XR_429385.2:n.853+21242G>T | ||
| XR_429386.2:n.854+21242G>T | ||
| XR_944075.1:n.865+21242G>T | ||
| XR_944076.1:n.861+21242G>T | ||
| XR_944077.1:n.865+21242G>T | ||
| XR_944078.1:n.865+21242G>T | ||
| XR_944079.1:n.855+21242G>T | ||
| XM_005268037.4:c.1893C>A | XP_005268094.1:p.Phe631Leu | |
| XM_011537119.2:c.1614C>A | XP_011535421.1:p.Phe538Leu | |
| XR_001751021.1:n.2753+21242G>T | ||
| XR_001751022.1:n.2753+21242G>T | ||
| XR_001751023.1:n.2753+21242G>T | ||
| XR_944075.3:n.929+21242G>T | ||
| NM_000369.4:c.1893C>A | NP_000360.2:p.Phe631Leu | |
| NM_000369.5:c.1893C>A MANE Select | NP_000360.2:p.Phe631Leu |