Revel Score:
ENST00000338581
0.460
ENST00000339598 (MANE Plus Clinical)
0.460
ENST00000402415
0.460
ENST00000272371 (MANE Select)
0.460
ENST00000403946
0.460
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00005136 (SAS)
Exomes Max Group AF
0.00005395 (SAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26461897C>T , CM000664.2:g.26461897C>T | GRCh38 |
| NC_000002.11:g.26684765C>T , CM000664.1:g.26684765C>T | GRCh37 |
| NC_000002.10:g.26538269C>T | NCBI36 |
| NG_009937.1:g.101802G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000272371.7:c.5332G>A MANE Select | ENSP00000272371.2:p.Val1778Ile | |
| ENST00000339598.8:c.3031G>A MANE Plus Clinical | ENSP00000344521.3:p.Val1011Ile | |
| ENST00000402415.8:c.3091G>A | ENSP00000383906.4:p.Val1031Ile | |
| ENST00000272371.6:c.5332G>A | ENSP00000272371.2:p.Val1778Ile | |
| ENST00000338581.10:c.3031G>A | ENSP00000345137.6:p.Val1011Ile | |
| ENST00000339598.7:c.3031G>A | ENSP00000344521.3:p.Val1011Ile | |
| ENST00000402415.7:c.3262G>A | ENSP00000383906.3:p.Val1088Ile | |
| ENST00000403946.7:c.5332G>A | ENSP00000385255.3:p.Val1778Ile | |
| NM_001287489.1:c.5332G>A | NP_001274418.1:p.Val1778Ile | |
| NM_004802.3:c.3031G>A | NP_004793.2:p.Val1011Ile | |
| NM_194248.2:c.5332G>A | NP_919224.1:p.Val1778Ile | |
| NM_194322.2:c.3262G>A | NP_919303.1:p.Val1088Ile | |
| NM_194323.2:c.3031G>A | NP_919304.1:p.Val1011Ile | |
| XM_005264644.2:c.5317G>A | XP_005264701.1:p.Val1773Ile | |
| XM_011533185.1:c.5377G>A | XP_011531487.1:p.Val1793Ile | |
| XM_017005338.1:c.5272G>A | XP_016860827.1:p.Val1758Ile | |
| NM_001287489.2:c.5332G>A | NP_001274418.1:p.Val1778Ile | |
| NM_004802.4:c.3031G>A | NP_004793.2:p.Val1011Ile | |
| NM_194248.3:c.5332G>A MANE Select | NP_919224.1:p.Val1778Ile | |
| NM_194322.3:c.3262G>A | NP_919303.1:p.Val1088Ile | |
| NM_194323.3:c.3031G>A MANE Plus Clinical | NP_919304.1:p.Val1011Ile |