Revel Score:
ENST00000298229 (MANE Select)
0.913
ENST00000541756
0.913
ENST00000538751
0.913
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.72233471C>T , CM000673.2:g.72233471C>T | GRCh38 |
| NC_000011.9:g.71944515C>T , CM000673.1:g.71944515C>T | GRCh37 |
| NC_000011.8:g.71622163C>T | NCBI36 |
| NG_023253.1:g.13634C>T | |
| NG_023253.2:g.13634C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000298229.7:c.2071C>T MANE Select | ENSP00000298229.2:p.Arg691Trp | |
| ENST00000298229.6:c.2071C>T | ENSP00000298229.2:p.Arg691Trp | |
| ENST00000538751.5:c.1345C>T | ENSP00000444619.1:p.Arg449Trp | |
| ENST00000541303.5:n.677C>T | ||
| ENST00000541756.5:c.1873C>T | ENSP00000446360.2:p.Arg625Trp | |
| ENST00000545355.5:n.224C>T | ||
| NM_001567.3:c.2071C>T | NP_001558.3:p.Arg691Trp | |
| XM_005273978.3:c.2137C>T | XP_005274035.1:p.Arg713Trp | |
| XM_005273979.3:c.2137C>T | XP_005274036.1:p.Arg713Trp | |
| XM_011544999.1:c.2071C>T | XP_011543301.1:p.Arg691Trp | |
| XM_011545000.1:c.2137C>T | XP_011543302.1:p.Arg713Trp | |
| XM_005273979.4:c.2137C>T | XP_005274036.1:p.Arg713Trp | |
| XM_011544999.2:c.2071C>T | XP_011543301.1:p.Arg691Trp | |
| XM_024448501.1:c.2137C>T | XP_024304269.1:p.Arg713Trp | |
| XM_024448502.1:c.2137C>T | XP_024304270.1:p.Arg713Trp | |
| XM_024448503.1:c.2107C>T | XP_024304271.1:p.Arg703Trp | |
| XM_024448504.1:c.2071C>T | XP_024304272.1:p.Arg691Trp | |
| XM_024448505.1:c.2137C>T | XP_024304273.1:p.Arg713Trp | |
| NM_001567.4:c.2071C>T MANE Select | NP_001558.3:p.Arg691Trp |