Revel Score:
ENST00000335508 (MANE Select)
0.806
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.197402760G>T , CM000664.2:g.197402760G>T | GRCh38 |
| NC_000002.11:g.198267484G>T , CM000664.1:g.198267484G>T | GRCh37 |
| NC_000002.10:g.197975729G>T | NCBI36 |
| NG_032903.2:g.37288C>A , LRG_624:g.37288C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335508.11:c.1873C>A MANE Select | ENSP00000335321.6:p.Arg625Ser | |
| ENST00000470268.2:n.3757C>A | ||
| ENST00000652026.1:c.*2940C>A | ENSP00000498652.1:n.*2940C>A | |
| ENST00000652738.1:c.*2132C>A | ENSP00000499119.1:n.*2132C>A | |
| ENST00000335508.10:c.1873C>A | ENSP00000335321.5:p.Arg625Ser | |
| NM_012433.2:c.1873C>A | NP_036565.2:p.Arg625Ser | |
| NM_012433.3:c.1873C>A , LRG_624t2:c.1873C>A | NP_036565.2:p.Arg625Ser | |
| XM_011510867.1:c.1435C>A | XP_011509169.1:p.Arg479Ser | |
| XM_011510868.1:c.1435C>A | XP_011509170.1:p.Arg479Ser | |
| XR_241300.2:n.1965C>A | ||
| XR_001738680.2:n.1918C>A | ||
| NM_012433.4:c.1873C>A MANE Select | NP_036565.2:p.Arg625Ser |