Revel Score:
ENST00000335295 (MANE Select)
0.800
ENST00000380315
0.800
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226720T>C , CM000673.2:g.5226720T>C | GRCh38 |
| NC_000011.9:g.5247950T>C , CM000673.1:g.5247950T>C | GRCh37 |
| NC_000011.8:g.5204526T>C | NCBI36 |
| NG_000007.3:g.70896A>G | |
| NG_059281.1:g.5352A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.172A>G | ENSP00000494175.1:p.Asn58Asp | |
| ENST00000335295.4:c.172A>G MANE Select | ENSP00000333994.3:p.Asn58Asp | |
| ENST00000380315.2:c.172A>G | ENSP00000369671.2:p.Asn58Asp | |
| ENST00000475226.1:n.104A>G | ||
| ENST00000485743.1:n.223A>G | ||
| ENST00000633227.1:c.156A>G | ENSP00000488004.1:p.Ala52= | |
| NM_000518.4:c.172A>G | NP_000509.1:p.Asn58Asp | |
| NM_000518.5:c.172A>G MANE Select | NP_000509.1:p.Asn58Asp |