Revel Score:
ENST00000375320
0.087
ENST00000359492
0.087
ENST00000375329
0.087
ENST00000375323
0.087
ENST00000236850 (MANE Select)
0.087
gnomAD v2:
gnomAD v4:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116836023G>T , CM000673.2:g.116836023G>T | GRCh38 |
| NC_000011.9:g.116706739G>T , CM000673.1:g.116706739G>T | GRCh37 |
| NC_000011.8:g.116211949G>T | NCBI36 |
| NG_012021.1:g.6600C>A , LRG_767:g.6600C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000236850.5:c.589C>A MANE Select | ENSP00000236850.3:p.Arg197Ser | |
| ENST00000236850.4:c.589C>A | ENSP00000236850.3:p.Arg197Ser | |
| ENST00000359492.6:c.589C>A | ENSP00000352471.2:p.Arg197Ser | |
| ENST00000375320.5:c.589C>A | ENSP00000364469.1:p.Arg197Ser | |
| ENST00000375323.5:c.589C>A | ENSP00000364472.1:p.Arg197Ser | |
| ENST00000375329.6:c.523C>A | ENSP00000364478.2:p.Arg175Ser | |
| NM_000039.1:c.589C>A , LRG_767t1:c.589C>A | NP_000030.1:p.Arg197Ser | |
| XM_005271539.2:c.589C>A | XP_005271596.1:p.Arg197Ser | |
| XM_005271540.1:c.589C>A | XP_005271597.1:p.Arg197Ser | |
| NM_000039.2:c.589C>A | NP_000030.1:p.Arg197Ser | |
| NM_001318017.1:c.589C>A | NP_001304946.1:p.Arg197Ser | |
| NM_001318018.1:c.589C>A | NP_001304947.1:p.Arg197Ser | |
| NM_001318021.1:c.262C>A | NP_001304950.1:p.Arg88Ser | |
| NM_001318017.2:c.589C>A | NP_001304946.1:p.Arg197Ser | |
| NM_001318018.2:c.589C>A | NP_001304947.1:p.Arg197Ser | |
| NM_000039.3:c.589C>A MANE Select | NP_000030.1:p.Arg197Ser |