Revel Score:
ENST00000376701 (MANE Select)
0.933
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.48689434G>C , CM000685.2:g.48689434G>C | GRCh38 |
| NC_000023.10:g.48547823G>C , CM000685.1:g.48547823G>C | GRCh37 |
| NC_000023.9:g.48432767G>C | NCBI36 |
| NG_007877.1:g.10638G>C , LRG_125:g.10638G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698625.1:c.1453G>C | ENSP00000513844.1:p.Asp485His | |
| ENST00000698626.1:c.1453G>C | ENSP00000513845.1:p.Gly485Arg | |
| ENST00000698635.1:c.1453G>C | ENSP00000513850.1:p.Gly485Arg | |
| ENST00000376701.5:c.1453G>C MANE Select | ENSP00000365891.4:p.Asp485His | |
| ENST00000376701.4:c.1453G>C | ENSP00000365891.4:p.Asp485His | |
| ENST00000470107.1:n.162G>C | ||
| NM_000377.2:c.1453G>C , LRG_125t1:c.1453G>C | NP_000368.1:p.Asp485His | |
| XM_011543977.1:c.1297G>C | XP_011542279.1:p.Asp433His | |
| XM_011543977.2:c.1297G>C | XP_011542279.1:p.Asp433His | |
| XM_017029786.1:c.1453G>C | XP_016885275.1:p.Gly485Arg | |
| NM_000377.3:c.1453G>C MANE Select | NP_000368.1:p.Asp485His |