Revel Score:
ENST00000324559 (MANE Select)
0.501
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.22255400C>G , CM000673.2:g.22255400C>G | GRCh38 |
| NC_000011.9:g.22276946C>G , CM000673.1:g.22276946C>G | GRCh37 |
| NC_000011.8:g.22233522C>G | NCBI36 |
| NG_015844.1:g.67225C>G , LRG_868:g.67225C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682089.1:n.530C>G | ||
| ENST00000682266.1:c.760C>G | ENSP00000507766.1:p.Arg254Gly | |
| ENST00000682341.1:c.1168C>G | ENSP00000508251.1:p.Arg390Gly | |
| ENST00000682530.1:c.*1142C>G | ENSP00000506805.1:n.*1142C>G | |
| ENST00000683197.1:c.1168C>G | ENSP00000507641.1:p.Arg390Gly | |
| ENST00000683411.1:c.760C>G | ENSP00000508397.1:p.Arg254Gly | |
| ENST00000683437.1:c.760C>G | ENSP00000508408.1:p.Arg254Gly | |
| ENST00000683613.1:n.2204C>G | ||
| ENST00000683834.1:n.1410C>G | ||
| ENST00000684663.1:c.1165C>G | ENSP00000508009.1:p.Arg389Gly | |
| ENST00000324559.9:c.1210C>G MANE Select | ENSP00000315371.9:p.Arg404Gly | |
| ENST00000648804.1:n.1545C>G | ||
| ENST00000324559.8:c.1210C>G | ENSP00000315371.8:p.Arg404Gly | |
| NM_001142649.1:c.1207C>G | NP_001136121.1:p.Arg403Gly | |
| NM_213599.2:c.1210C>G , LRG_868t1:c.1210C>G | NP_998764.1:p.Arg404Gly | |
| XM_005252820.2:c.1168C>G | XP_005252877.2:p.Arg390Gly | |
| XM_005252821.2:c.1165C>G | XP_005252878.2:p.Arg389Gly | |
| XM_005252822.3:c.1132C>G | XP_005252879.1:p.Arg378Gly | |
| XM_005252823.3:c.1129C>G | XP_005252880.1:p.Arg377Gly | |
| XM_011519949.1:c.1117C>G | XP_011518251.1:p.Arg373Gly | |
| XM_005252820.3:c.1168C>G | XP_005252877.2:p.Arg390Gly | |
| XM_005252821.3:c.1165C>G | XP_005252878.2:p.Arg389Gly | |
| XM_005252822.4:c.1132C>G | XP_005252879.1:p.Arg378Gly | |
| XM_011519949.2:c.1117C>G | XP_011518251.1:p.Arg373Gly | |
| NM_001142649.2:c.1207C>G | NP_001136121.1:p.Arg403Gly | |
| NM_213599.3:c.1210C>G MANE Select | NP_998764.1:p.Arg404Gly |