Revel Score:
ENST00000262464 (MANE Select)
0.628
ENST00000508053
0.628
ENST00000507835
0.628
ENST00000508989
0.628
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128335465T>A , CM000667.2:g.128335465T>A | GRCh38 |
| NC_000005.9:g.127671157T>A , CM000667.1:g.127671157T>A | GRCh37 |
| NC_000005.8:g.127699056T>A | NCBI36 |
| NG_008750.1:g.207579A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.621A>T | ||
| ENST00000703785.1:n.702A>T | ||
| ENST00000262464.9:c.3837A>T MANE Select | ENSP00000262464.4:p.Arg1279Ser | |
| ENST00000262464.8:c.3837A>T | ENSP00000262464.4:p.Arg1279Ser | |
| ENST00000507835.5:c.387A>T | ENSP00000426839.1:p.Arg129Ser | |
| ENST00000508053.5:c.3837A>T | ENSP00000424571.1:p.Arg1279Ser | |
| ENST00000508989.5:c.3738A>T | ENSP00000425596.1:p.Arg1246Ser | |
| ENST00000619499.4:c.3834A>T | ENSP00000482132.1:p.Arg1278Ser | |
| NM_001999.3:c.3837A>T | NP_001990.2:p.Arg1279Ser | |
| XM_017009228.2:c.3684A>T | XP_016864717.1:p.Arg1228Ser | |
| NM_001999.4:c.3837A>T MANE Select | NP_001990.2:p.Arg1279Ser |