Revel Score:
ENST00000370396 (MANE Select)
0.944
ENST00000542741
0.944
ENST00000543350
0.944
ENST00000413012
0.944
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.150657887C>G , CM000685.2:g.150657887C>G | GRCh38 |
| NC_000023.10:g.149826360C>G , CM000685.1:g.149826360C>G | GRCh37 |
| NC_000023.9:g.149577018C>G | NCBI36 |
| NG_008199.1:g.94314C>G , LRG_839:g.94314C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684910.1:c.*653C>G | ENSP00000509844.1:n.*653C>G | |
| ENST00000685439.1:c.775C>G | ENSP00000508454.1:p.His259Asp | |
| ENST00000685944.1:c.1120C>G | ENSP00000509266.1:p.His374Asp | |
| ENST00000686212.1:n.722C>G | ||
| ENST00000687215.1:c.*875C>G | ENSP00000509706.1:n.*875C>G | |
| ENST00000688152.1:c.*564C>G | ENSP00000509360.1:n.*564C>G | |
| ENST00000688403.1:c.376C>G | ENSP00000508944.1:p.His126Asp | |
| ENST00000689314.1:c.1165C>G | ENSP00000510607.1:p.His389Asp | |
| ENST00000689694.1:c.1120C>G | ENSP00000508718.1:p.His374Asp | |
| ENST00000689810.1:c.*769C>G | ENSP00000510635.1:n.*769C>G | |
| ENST00000690282.1:c.376C>G | ENSP00000509809.1:p.His126Asp | |
| ENST00000690351.1:c.*772C>G | ENSP00000509728.1:n.*772C>G | |
| ENST00000691232.1:c.775C>G | ENSP00000509675.1:p.His259Asp | |
| ENST00000691482.1:n.2135C>G | ||
| ENST00000691686.1:c.1120C>G | ENSP00000509784.1:p.His374Asp | |
| ENST00000691851.1:c.1053+7986C>G | ENSP00000510106.1:n.1053+7986C>G | |
| ENST00000692015.1:c.907C>G | ENSP00000510634.1:p.His303Asp | |
| ENST00000692638.1:c.*925C>G | ENSP00000509412.1:n.*925C>G | |
| ENST00000692852.1:c.931C>G | ENSP00000510337.1:p.His311Asp | |
| ENST00000692915.1:c.*1266C>G | ENSP00000508547.1:n.*1266C>G | |
| ENST00000370396.7:c.1120C>G MANE Select | ENSP00000359423.3:p.His374Asp | |
| ENST00000306167.11:n.987C>G | ||
| ENST00000370396.6:c.1120C>G | ENSP00000359423.2:p.His374Asp | |
| NM_000252.2:c.1120C>G , LRG_839t1:c.1120C>G | NP_000243.1:p.His374Asp | |
| XM_005274687.2:c.1120C>G | XP_005274744.1:p.His374Asp | |
| XM_011531170.1:c.1186C>G | XP_011529472.1:p.His396Asp | |
| XM_011531171.1:c.1165C>G | XP_011529473.1:p.His389Asp | |
| XM_011531172.1:c.1165C>G | XP_011529474.1:p.His389Asp | |
| XM_011531173.1:c.1120C>G | XP_011529475.1:p.His374Asp | |
| XM_011531173.2:c.1120C>G | XP_011529475.1:p.His374Asp | |
| XM_017029547.1:c.1165C>G | XP_016885036.1:p.His389Asp | |
| XM_017029548.1:c.1165C>G | XP_016885037.1:p.His389Asp | |
| XM_017029549.1:c.1120C>G | XP_016885038.1:p.His374Asp | |
| XM_017029550.1:c.1009C>G | XP_016885039.1:p.His337Asp | |
| XM_017029551.2:c.376C>G | XP_016885040.1:p.His126Asp | |
| NM_000252.3:c.1120C>G MANE Select | NP_000243.1:p.His374Asp | |
| NM_001376906.1:c.1120C>G | NP_001363835.1:p.His374Asp | |
| NM_001376907.1:c.1009C>G | NP_001363836.1:p.His337Asp | |
| NM_001376908.1:c.1120C>G | NP_001363837.1:p.His374Asp |