Revel Score:
ENST00000263321 (MANE Select)
0.726
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.89191364G>C , CM000673.2:g.89191364G>C | GRCh38 |
| NC_000011.9:g.88924532G>C , CM000673.1:g.88924532G>C | GRCh37 |
| NC_000011.8:g.88564180G>C | NCBI36 |
| NG_008748.1:g.18493G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263321.6:c.982G>C MANE Select | ENSP00000263321.4:p.Glu328Gln | |
| ENST00000263321.5:c.982G>C | ENSP00000263321.4:p.Glu328Gln | |
| ENST00000526139.1:n.1043G>C | ||
| NM_000372.4:c.982G>C | NP_000363.1:p.Glu328Gln | |
| XM_011542970.1:c.982G>C | XP_011541272.1:p.Glu328Gln | |
| XM_011542970.2:c.982G>C | XP_011541272.1:p.Glu328Gln | |
| XR_001748321.1:n.2718-77831C>G | ||
| XR_001748322.1:n.2733-77831C>G | ||
| NM_000372.5:c.982G>C MANE Select | NP_000363.1:p.Glu328Gln |