Revel Score:
ENST00000335295 (MANE Select)
0.341
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225622A>C , CM000673.2:g.5225622A>C | GRCh38 |
| NC_000011.9:g.5246852A>C , CM000673.1:g.5246852A>C | GRCh37 |
| NC_000011.8:g.5203428A>C | NCBI36 |
| NG_000007.3:g.71994T>G | |
| NG_059281.1:g.6450T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.420T>G | ENSP00000494175.1:p.Asn140Lys | |
| ENST00000335295.4:c.420T>G MANE Select | ENSP00000333994.3:p.Asn140Lys | |
| ENST00000633227.1:c.*236T>G | ENSP00000488004.1:n.*236T>G | |
| NM_000518.4:c.420T>G | NP_000509.1:p.Asn140Lys | |
| NM_000518.5:c.420T>G MANE Select | NP_000509.1:p.Asn140Lys |