Revel Score:
ENST00000399402
0.832
ENST00000307363 (MANE Select)
0.832
ENST00000445488
0.832
ENST00000307377
0.832
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.0000727 (EAS)
Exomes Max Group AF
0.00008205 (EAS)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33018452T>A , CM000665.2:g.33018452T>A | GRCh38 |
| NC_000003.11:g.33059944T>A , CM000665.1:g.33059944T>A | GRCh37 |
| NC_000003.10:g.33034948T>A | NCBI36 |
| NG_009005.1:g.83751A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.1343A>T MANE Select | ENSP00000306920.4:p.Asp448Val | |
| ENST00000307363.9:c.1343A>T | ENSP00000306920.4:p.Asp448Val | |
| ENST00000307377.12:c.950A>T | ENSP00000305920.8:p.Asp317Val | |
| ENST00000399402.7:c.1253A>T | ENSP00000382333.2:p.Asp418Val | |
| ENST00000461475.5:n.442A>T | ||
| ENST00000467571.5:n.380A>T | ||
| ENST00000497796.5:n.595A>T | ||
| NM_000404.2:c.1343A>T | NP_000395.2:p.Asp448Val | |
| NM_000404.3:c.1343A>T | NP_000395.2:p.Asp448Val | |
| NM_001079811.1:c.1253A>T | NP_001073279.1:p.Asp418Val | |
| NM_001079811.2:c.1253A>T | NP_001073279.1:p.Asp418Val | |
| NM_001135602.1:c.950A>T | NP_001129074.1:p.Asp317Val | |
| NM_001135602.2:c.950A>T | NP_001129074.1:p.Asp317Val | |
| NM_001317040.1:c.1487A>T | NP_001303969.1:p.Asp496Val | |
| NM_000404.4:c.1343A>T MANE Select | NP_000395.3:p.Asp448Val | |
| NM_001079811.3:c.1253A>T | NP_001073279.2:p.Asp418Val | |
| NM_001135602.3:c.950A>T | NP_001129074.2:p.Asp317Val | |
| NM_001317040.2:c.1487A>T | NP_001303969.2:p.Asp496Val | |
| NM_001393580.1:c.1343A>T | NP_001380509.1:p.Asp448Val |