Revel Score:
ENST00000381913
0.865
ENST00000301365
0.865
ENST00000430263
0.865
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.3518644G>A , CM000679.2:g.3518644G>A | GRCh38 |
| NC_000017.10:g.3421938G>A , CM000679.1:g.3421938G>A | GRCh37 |
| NC_000017.9:g.3368688G>A | NCBI36 |
| NG_032144.2:g.44352C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000576742.6:c.2017C>T MANE Select | ENSP00000461518.2:p.Leu673Phe | |
| ENST00000301365.8:c.2017C>T | ENSP00000301365.4:p.Leu673Phe | |
| ENST00000381913.8:c.1279C>T | ||
| ENST00000571139.5:c.*2009C>T | ENSP00000458187.1:n.*2009C>T | |
| ENST00000572519.1:c.2017C>T | ENSP00000460215.1:p.Leu673Phe | |
| ENST00000573539.5:c.*2027C>T | ENSP00000458239.1:n.*2027C>T | |
| ENST00000576742.5:c.2017C>T | ENSP00000461518.1:p.Leu673Phe | |
| ENST00000577016.5:c.535C>T | ||
| ENST00000616411.4:c.1969C>T | ENSP00000483947.1:p.Leu657Phe | |
| NM_001258205.1:c.2017C>T | NP_001245134.1:p.Leu673Phe | |
| NM_145068.3:c.2017C>T | NP_659505.1:p.Leu673Phe | |
| XM_011523693.1:c.*95C>T | XP_011521995.1:n.*95C>T | |
| XM_011523694.1:c.1312C>T | XP_011521996.1:p.Leu438Phe | |
| XM_011523695.1:c.970C>T | XP_011521997.1:p.Leu324Phe | |
| XR_934004.1:n.2091C>T | ||
| NM_001258205.2:c.2017C>T | NP_001245134.1:p.Leu673Phe | |
| NM_145068.4:c.2017C>T MANE Select | NP_659505.1:p.Leu673Phe |