Revel Score:
ENST00000308868 (MANE Select)
0.550
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.128254440G>A , CM000669.2:g.128254440G>A | GRCh38 |
| NC_000007.13:g.127894493G>A , CM000669.1:g.127894493G>A | GRCh37 |
| NC_000007.12:g.127681729G>A | NCBI36 |
| NG_007450.1:g.18163G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000308868.5:c.181G>A MANE Select | ENSP00000312652.4:p.Asp61Asn | |
| ENST00000308868.4:c.181G>A | ENSP00000312652.4:p.Asp61Asn | |
| NM_000230.2:c.181G>A | NP_000221.1:p.Asp61Asn | |
| XM_005250340.3:c.178G>A | XP_005250397.1:p.Asp60Asn | |
| XM_005250340.5:c.178G>A | XP_005250397.1:p.Asp60Asn | |
| NM_000230.3:c.181G>A MANE Select | NP_000221.1:p.Asp61Asn |