Revel Score:
ENST00000265433 (MANE Select)
0.068
ENST00000409330
0.068
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00000553 (AMR)
Exomes Max Group AF
0.00000741 (AMR)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.89953498T>C , CM000670.2:g.89953498T>C | GRCh38 |
| NC_000008.10:g.90965726T>C , CM000670.1:g.90965726T>C | GRCh37 |
| NC_000008.9:g.91034902T>C | NCBI36 |
| NG_008860.1:g.36174A>G , LRG_158:g.36174A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000494804.2:n.2893A>G | ||
| ENST00000517337.2:c.1345A>G | ENSP00000429971.2:p.Ile449Val | |
| ENST00000523444.2:c.1345A>G | ENSP00000428252.2:p.Ile449Val | |
| ENST00000697292.1:c.1591A>G | ENSP00000513229.1:p.Ile531Val | |
| ENST00000697293.1:c.1591A>G | ENSP00000513230.1:p.Ile531Val | |
| ENST00000697294.1:c.*1202A>G | ENSP00000513231.1:n.*1202A>G | |
| ENST00000697295.1:c.*900A>G | ENSP00000513232.1:n.*900A>G | |
| ENST00000697296.1:c.*1259A>G | ENSP00000513233.1:n.*1259A>G | |
| ENST00000697297.1:n.3376A>G | ||
| ENST00000697298.1:c.1345A>G | ENSP00000513234.1:p.Ile449Val | |
| ENST00000697299.1:c.1345A>G | ENSP00000513235.1:p.Ile449Val | |
| ENST00000697300.1:c.*1195A>G | ENSP00000513236.1:n.*1195A>G | |
| ENST00000697301.1:c.*1112A>G | ENSP00000513237.1:n.*1112A>G | |
| ENST00000697302.1:c.*1112A>G | ENSP00000513238.1:n.*1112A>G | |
| ENST00000697303.1:c.*1195A>G | ENSP00000513239.1:n.*1195A>G | |
| ENST00000697304.1:c.1279A>G | ENSP00000513240.1:p.Ile427Val | |
| ENST00000697306.1:c.*591A>G | ENSP00000513241.1:n.*591A>G | |
| ENST00000697307.1:c.1591A>G | ENSP00000513242.1:p.Ile531Val | |
| ENST00000697308.1:c.1591A>G | ENSP00000513243.1:p.Ile531Val | |
| ENST00000697309.1:c.1591A>G | ENSP00000513244.1:p.Ile531Val | |
| ENST00000697310.1:c.1591A>G | ENSP00000513245.1:p.Ile531Val | |
| ENST00000697311.1:c.1591A>G | ENSP00000513246.1:p.Ile531Val | |
| ENST00000697312.1:c.*989A>G | ENSP00000513247.1:n.*989A>G | |
| ENST00000697313.1:n.2687+16866A>G | ||
| ENST00000697314.1:n.3382A>G | ||
| ENST00000697315.1:c.1591A>G | ENSP00000513248.1:p.Ile531Val | |
| ENST00000697316.1:n.1712A>G | ||
| ENST00000697317.1:n.1701A>G | ||
| ENST00000697318.1:n.1703A>G | ||
| ENST00000265433.8:c.1591A>G MANE Select | ENSP00000265433.4:p.Ile531Val | |
| ENST00000265433.7:c.1591A>G | ENSP00000265433.3:p.Ile531Val | |
| ENST00000396252.6:c.*1464A>G | ENSP00000379551.2:n.*1464A>G | |
| ENST00000409330.5:c.1345A>G | ENSP00000386924.1:p.Ile449Val | |
| NM_001024688.2:c.1345A>G | NP_001019859.1:p.Ile449Val | |
| NM_002485.4:c.1591A>G , LRG_158t1:c.1591A>G | NP_002476.2:p.Ile531Val | |
| XM_011517044.1:c.1567A>G | XP_011515346.1:p.Ile523Val | |
| XM_011517045.1:c.1345A>G | XP_011515347.1:p.Ile449Val | |
| XR_928335.1:n.1730A>G | ||
| XM_017013460.1:c.712A>G | XP_016868949.1:p.Ile238Val | |
| XM_017013462.2:c.712A>G | XP_016868951.1:p.Ile238Val | |
| XM_024447163.1:c.1345A>G | XP_024302931.1:p.Ile449Val | |
| XM_024447164.1:c.1345A>G | XP_024302932.1:p.Ile449Val | |
| XM_024447165.1:c.712A>G | XP_024302933.1:p.Ile238Val | |
| NM_002485.5:c.1591A>G MANE Select | NP_002476.2:p.Ile531Val | |
| NM_001024688.3:c.1345A>G | NP_001019859.1:p.Ile449Val |