Revel Score:
ENST00000445590 (MANE Select)
0.039
ENST00000360827
0.039
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.222750009A>C , CM000663.2:g.222750009A>C | GRCh38 |
| NC_000001.10:g.222923351A>C , CM000663.1:g.222923351A>C | GRCh37 |
| NC_000001.9:g.220989974A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000445590.4:c.428A>C MANE Select | ENSP00000414451.2:p.Gln143Pro | |
| ENST00000360827.6:c.428A>C | ENSP00000354070.2:p.Gln143Pro | |
| ENST00000391880.6:c.*569A>C | ENSP00000375752.2:n.*569A>C | |
| ENST00000445590.3:c.428A>C | ENSP00000414451.2:p.Gln143Pro | |
| NM_207468.2:c.428A>C | NP_997351.2:p.Gln143Pro | |
| XM_006711318.2:c.241+2928A>C | XP_006711381.1:n.241+2928A>C | |
| NM_001324080.1:c.428A>C | NP_001311009.1:p.Gln143Pro | |
| NR_136691.1:n.1198A>C | ||
| XM_017001279.1:c.428A>C | XP_016856768.1:p.Gln143Pro | |
| XM_017001280.1:c.428A>C | XP_016856769.1:p.Gln143Pro | |
| XM_017001281.1:c.428A>C | XP_016856770.1:p.Gln143Pro | |
| XM_017001282.1:c.428A>C | XP_016856771.1:p.Gln143Pro | |
| XM_017001285.1:c.274+2928A>C | XP_016856774.1:n.274+2928A>C | |
| NM_001324080.2:c.428A>C | NP_001311009.1:p.Gln143Pro | |
| NM_207468.3:c.428A>C | NP_997351.2:p.Gln143Pro | |
| NR_136691.2:n.1212A>C | ||
| NM_001394345.1:c.428A>C MANE Select | NP_001381274.1:p.Gln143Pro |