Revel Score:
ENST00000446804
0.045
ENST00000311907 (MANE Select)
0.380
ENST00000530231
0.380
ENST00000442468
0.380
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46725908T>G , CM000673.2:g.46725908T>G | GRCh38 |
| NC_000011.9:g.46747458T>G , CM000673.1:g.46747458T>G | GRCh37 |
| NC_000011.8:g.46704034T>G | NCBI36 |
| NG_008953.1:g.11716T>G , LRG_551:g.11716T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000311907.10:c.609T>G MANE Select | ENSP00000308541.5:p.Ser203Arg | |
| ENST00000311907.9:c.609T>G | ENSP00000308541.5:p.Ser203Arg | |
| ENST00000442468.1:c.579T>G | ENSP00000387413.1:p.Ser193Arg | |
| ENST00000490274.1:n.389T>G | ||
| ENST00000530231.5:c.609T>G | ENSP00000433907.1:p.Ser203Arg | |
| NM_000506.3:c.609T>G | NP_000497.1:p.Ser203Arg | |
| NM_000506.4:c.609T>G , LRG_551t1:c.609T>G | NP_000497.1:p.Ser203Arg | |
| NM_001311257.1:c.561T>G | NP_001298186.1:p.Ser187Arg | |
| XR_428840.2:n.653T>G | ||
| XR_428840.4:n.644T>G | ||
| NM_000506.5:c.609T>G MANE Select | NP_000497.1:p.Ser203Arg | |
| NM_001311257.2:c.561T>G | NP_001298186.1:p.Ser187Arg |