Revel Score:
ENST00000371817 (MANE Select)
0.638
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00004781 (NFE)
Exomes Max Group AF
0.00004986 (NFE)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.134700037C>T , CM000671.2:g.134700037C>T | GRCh38 |
| NC_000009.11:g.137591883C>T , CM000671.1:g.137591883C>T | GRCh37 |
| NC_000009.10:g.136731704C>T | NCBI36 |
| NG_008030.1:g.63232C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371820.4:c.406C>T | ENSP00000360885.4:p.Pro136Ser | |
| ENST00000371817.8:c.406C>T MANE Select | ENSP00000360882.3:p.Pro136Ser | |
| ENST00000371817.7:c.406C>T | ENSP00000360882.3:p.Pro136Ser | |
| ENST00000464187.1:n.828C>T | ||
| ENST00000618395.4:c.406C>T | ENSP00000481360.1:p.Pro136Ser | |
| NM_000093.4:c.406C>T | NP_000084.3:p.Pro136Ser | |
| NM_001278074.1:c.406C>T | NP_001265003.1:p.Pro136Ser | |
| XR_929712.1:n.808C>T | ||
| XR_929713.1:n.808C>T | ||
| XM_017014266.2:c.406C>T | XP_016869755.1:p.Pro136Ser | |
| XR_001746183.1:n.804C>T | ||
| NM_000093.5:c.406C>T MANE Select | NP_000084.3:p.Pro136Ser |