Revel Score:
ENST00000534884
0.132
ENST00000378682
0.132
ENST00000378684
0.132
ENST00000378677
0.132
ENST00000357033 (MANE Select)
0.132
ENST00000542849
0.132
ENST00000535280
0.132
gnomAD v2:
gnomAD v4:
Joint Max Group AF
0.00001737 (AMR)
Exomes Max Group AF
0.00002268 (AMR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.32310253C>T , CM000685.2:g.32310253C>T | GRCh38 |
| NC_000023.10:g.32328370C>T , CM000685.1:g.32328370C>T | GRCh37 |
| NC_000023.9:g.32238291C>T | NCBI36 |
| NG_012232.1:g.1034357G>A , LRG_199:g.1034357G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000358062.7:c.792G>A | ENSP00000350765.3:p.Met264Ile | |
| ENST00000357033.9:c.5946G>A MANE Select | ENSP00000354923.3:p.Met1982Ile | |
| ENST00000619831.5:c.1914G>A | ENSP00000479270.2:p.Met638Ile | |
| ENST00000357033.8:c.5946G>A | ENSP00000354923.3:p.Met1982Ile | |
| ENST00000378677.6:c.5934G>A | ENSP00000367948.2:p.Met1978Ile | |
| ENST00000488902.5:n.336-93190G>A | ||
| ENST00000619831.4:c.5934G>A | ENSP00000479270.1:p.Met1978Ile | |
| ENST00000620040.4:c.5946G>A | ENSP00000478150.1:p.Met1982Ile | |
| NM_000109.3:c.5922G>A | NP_000100.2:p.Met1974Ile | |
| NM_004006.2:c.5946G>A , LRG_199t1:c.5946G>A | NP_003997.1:p.Met1982Ile | |
| NM_004009.3:c.5934G>A | NP_004000.1:p.Met1978Ile | |
| NM_004010.3:c.5577G>A | NP_004001.1:p.Met1859Ile | |
| NM_004011.3:c.1923G>A | NP_004002.2:p.Met641Ile | |
| NM_004012.3:c.1914G>A | NP_004003.1:p.Met638Ile | |
| XM_006724468.2:c.5946G>A | XP_006724531.1:p.Met1982Ile | |
| XM_006724469.2:c.5922G>A | XP_006724532.1:p.Met1974Ile | |
| XM_006724470.2:c.5946G>A | XP_006724533.1:p.Met1982Ile | |
| XM_006724471.2:c.5946G>A | XP_006724534.1:p.Met1982Ile | |
| XM_006724472.2:c.5817G>A | XP_006724535.1:p.Met1939Ile | |
| XM_006724473.2:c.5808G>A | XP_006724536.1:p.Met1936Ile | |
| XM_006724474.2:c.5946G>A | XP_006724537.1:p.Met1982Ile | |
| XM_006724475.2:c.5946G>A | XP_006724538.1:p.Met1982Ile | |
| XM_011545467.1:c.5823G>A | XP_011543769.1:p.Met1941Ile | |
| XM_011545468.1:c.5946G>A | XP_011543770.1:p.Met1982Ile | |
| XM_006724469.3:c.5922G>A | XP_006724532.1:p.Met1974Ile | |
| XM_006724470.3:c.5946G>A | XP_006724533.1:p.Met1982Ile | |
| XM_006724474.3:c.5946G>A | XP_006724537.1:p.Met1982Ile | |
| XM_011545468.2:c.5946G>A | XP_011543770.1:p.Met1982Ile | |
| XM_017029328.1:c.5946G>A | XP_016884817.1:p.Met1982Ile | |
| XM_017029329.1:c.5946G>A | XP_016884818.1:p.Met1982Ile | |
| XM_017029330.2:c.5946G>A | XP_016884819.1:p.Met1982Ile | |
| XM_017029331.1:c.120G>A | XP_016884820.1:p.Met40Ile | |
| NM_000109.4:c.5922G>A | NP_000100.3:p.Met1974Ile | |
| NM_004006.3:c.5946G>A MANE Select | NP_003997.2:p.Met1982Ile | |
| NM_004011.4:c.1923G>A | NP_004002.3:p.Met641Ile | |
| NM_004012.4:c.1914G>A | NP_004003.2:p.Met638Ile |