Revel Score:
ENST00000426263 (MANE Select)
0.889
ENST00000372501
0.889
ENST00000397019
0.889
ENST00000439722
0.889
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.42929921G>A , CM000663.2:g.42929921G>A | GRCh38 |
| NC_000001.10:g.43395592G>A , CM000663.1:g.43395592G>A | GRCh37 |
| NC_000001.9:g.43168179G>A | NCBI36 |
| NG_008232.1:g.34256C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000426263.10:c.631C>T MANE Select | ENSP00000416293.2:p.Pro211Ser | |
| ENST00000669445.1:c.8C>T | ||
| ENST00000674765.1:c.631C>T | ENSP00000501811.1:p.Pro211Ser | |
| ENST00000675112.1:n.654C>T | ||
| ENST00000676254.1:n.1080C>T | ||
| ENST00000426263.7:c.631C>T | ENSP00000416293.2:p.Pro211Ser | |
| ENST00000439722.2:c.510C>T | ENSP00000395521.2:n.510C>T | |
| ENST00000475162.3:c.415+705C>T | ||
| ENST00000630287.2:c.517-141C>T | ENSP00000486694.1:n.517-141C>T | |
| NM_006516.2:c.631C>T | NP_006507.2:p.Pro211Ser | |
| NM_006516.3:c.631C>T | NP_006507.2:p.Pro211Ser | |
| NM_006516.4:c.631C>T MANE Select | NP_006507.2:p.Pro211Ser |