Revel Score:
ENST00000261405 (MANE Select)
0.582
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.6110484T>C , CM000674.2:g.6110484T>C | GRCh38 |
| NC_000012.11:g.6219650T>C , CM000674.1:g.6219650T>C | GRCh37 |
| NC_000012.10:g.6089911T>C | NCBI36 |
| NG_009072.1:g.19187A>G | |
| NG_009072.2:g.19187A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261405.10:c.422A>G MANE Select | ENSP00000261405.5:p.Asp141Gly | |
| ENST00000261405.9:c.422A>G | ENSP00000261405.5:p.Asp141Gly | |
| ENST00000321023.5:c.*481A>G | ENSP00000461331.1:n.*481A>G | |
| ENST00000538635.5:n.420+31A>G | ||
| NM_000552.3:c.422A>G | NP_000543.2:p.Asp141Gly | |
| NM_000552.4:c.422A>G | NP_000543.2:p.Asp141Gly | |
| NM_000552.5:c.422A>G MANE Select | NP_000543.3:p.Asp141Gly |