Revel Score:
ENST00000243644 (MANE Select)
0.189
ClinVar RCV:
ClinVar Variation:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.51965428C>T , CM000681.2:g.51965428C>T | GRCh38 |
| NC_000019.9:g.52468681C>T , CM000681.1:g.52468681C>T | GRCh37 |
| NC_000019.8:g.57160493C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000243644.9:c.1025G>A (ZNF350) MANE Select | ENSP00000243644.3:p.Gly342Glu | |
| ENST00000243644.8:c.1025G>A (ZNF350) | ENSP00000243644.3:p.Gly342Glu | |
| NM_021632.3:c.1025G>A (ZNF350) | NP_067645.3:p.Gly342Glu | |
| NR_103847.1:n.103-10963C>T (ZNF350-AS1) | ||
| XM_011527196.1:c.917G>A (ZNF350) | XP_011525498.1:p.Gly306Glu | |
| XM_017027094.1:c.1151G>A (ZNF350) | XP_016882583.1:p.Gly384Glu | |
| XM_017027095.1:c.1151G>A (ZNF350) | XP_016882584.1:p.Gly384Glu | |
| XM_017027096.1:c.1151G>A (ZNF350) | XP_016882585.1:p.Gly384Glu | |
| XM_017027098.1:c.1025G>A (ZNF350) | XP_016882587.1:p.Gly342Glu | |
| XM_017027099.1:c.1025G>A (ZNF350) | XP_016882588.1:p.Gly342Glu | |
| XM_017027100.1:c.1025G>A (ZNF350) | XP_016882589.1:p.Gly342Glu | |
| XM_017027101.1:c.347G>A (ZNF350) | XP_016882590.1:p.Gly116Glu | |
| XM_017027102.2:c.347G>A (ZNF350) | XP_016882591.1:p.Gly116Glu | |
| XM_017027103.2:c.347G>A (ZNF350) | XP_016882592.1:p.Gly116Glu | |
| XM_024451632.1:c.1043G>A (ZNF350) | XP_024307400.1:p.Gly348Glu | |
| XM_024451633.1:c.347G>A (ZNF350) | XP_024307401.1:p.Gly116Glu | |
| XM_024451634.1:c.347G>A (ZNF350) | XP_024307402.1:p.Gly116Glu | |
| XM_024451635.1:c.347G>A (ZNF350) | XP_024307403.1:p.Gly116Glu | |
| NM_021632.4:c.1025G>A (ZNF350) MANE Select | NP_067645.3:p.Gly342Glu |