Revel Score:
ENST00000264595 (MANE Select)
0.815
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.177442276A>T , CM000666.2:g.177442276A>T | GRCh38 |
| NC_000004.11:g.178363430A>T , CM000666.1:g.178363430A>T | GRCh37 |
| NC_000004.10:g.178600424A>T | NCBI36 |
| NG_011845.2:g.5228T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264595.7:c.100T>A MANE Select | ENSP00000264595.2:p.Trp34Arg | |
| ENST00000264595.6:c.100T>A | ENSP00000264595.2:p.Trp34Arg | |
| ENST00000506853.5:n.134T>A | ||
| ENST00000510955.5:n.134T>A | ||
| ENST00000511231.1:n.134T>A | ||
| NM_000027.3:c.100T>A | NP_000018.2:p.Trp34Arg | |
| NM_001171988.1:c.100T>A | NP_001165459.1:p.Trp34Arg | |
| NR_033655.1:n.228T>A | ||
| XM_006714123.2:c.100T>A | XP_006714186.1:p.Trp34Arg | |
| XR_001741155.2:n.194T>A | ||
| NM_000027.4:c.100T>A MANE Select | NP_000018.2:p.Trp34Arg | |
| NM_001171988.2:c.100T>A | NP_001165459.1:p.Trp34Arg | |
| NR_033655.2:n.162T>A |