Revel Score:
ENST00000370396 (MANE Select)
0.970
ENST00000542741
0.970
ENST00000543350
0.970
ENST00000413012
0.970
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.150645795T>G , CM000685.2:g.150645795T>G | GRCh38 |
| NC_000023.10:g.149814268T>G , CM000685.1:g.149814268T>G | GRCh37 |
| NC_000023.9:g.149564926T>G | NCBI36 |
| NG_008199.1:g.82222T>G , LRG_839:g.82222T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684910.1:c.*324T>G | ENSP00000509844.1:n.*324T>G | |
| ENST00000685439.1:c.446T>G | ENSP00000508454.1:p.Ile149Ser | |
| ENST00000685944.1:c.791T>G | ENSP00000509266.1:p.Ile264Ser | |
| ENST00000686212.1:n.393T>G | ||
| ENST00000687215.1:c.*546T>G | ENSP00000509706.1:n.*546T>G | |
| ENST00000688152.1:c.*235T>G | ENSP00000509360.1:n.*235T>G | |
| ENST00000688403.1:c.47T>G | ENSP00000508944.1:p.Ile16Ser | |
| ENST00000689314.1:c.836T>G | ENSP00000510607.1:p.Ile279Ser | |
| ENST00000689694.1:c.791T>G | ENSP00000508718.1:p.Ile264Ser | |
| ENST00000689810.1:c.*440T>G | ENSP00000510635.1:n.*440T>G | |
| ENST00000690282.1:c.47T>G | ENSP00000509809.1:p.Ile16Ser | |
| ENST00000690351.1:c.*443T>G | ENSP00000509728.1:n.*443T>G | |
| ENST00000691232.1:c.446T>G | ENSP00000509675.1:p.Ile149Ser | |
| ENST00000691482.1:n.1806T>G | ||
| ENST00000691686.1:c.791T>G | ENSP00000509784.1:p.Ile264Ser | |
| ENST00000691851.1:c.791T>G | ENSP00000510106.1:p.Ile264Ser | |
| ENST00000692015.1:c.578T>G | ENSP00000510634.1:p.Ile193Ser | |
| ENST00000692638.1:c.*596T>G | ENSP00000509412.1:n.*596T>G | |
| ENST00000692852.1:c.679-3921T>G | ENSP00000510337.1:n.679-3921T>G | |
| ENST00000692915.1:c.*998T>G | ENSP00000508547.1:n.*998T>G | |
| ENST00000370396.7:c.791T>G MANE Select | ENSP00000359423.3:p.Ile264Ser | |
| ENST00000306167.11:n.658T>G | ||
| ENST00000370396.6:c.791T>G | ENSP00000359423.2:p.Ile264Ser | |
| ENST00000490530.1:n.730T>G | ||
| NM_000252.2:c.791T>G , LRG_839t1:c.791T>G | NP_000243.1:p.Ile264Ser | |
| XM_005274687.2:c.791T>G | XP_005274744.1:p.Ile264Ser | |
| XM_011531170.1:c.857T>G | XP_011529472.1:p.Ile286Ser | |
| XM_011531171.1:c.836T>G | XP_011529473.1:p.Ile279Ser | |
| XM_011531172.1:c.836T>G | XP_011529474.1:p.Ile279Ser | |
| XM_011531173.1:c.791T>G | XP_011529475.1:p.Ile264Ser | |
| XM_011531173.2:c.791T>G | XP_011529475.1:p.Ile264Ser | |
| XM_017029547.1:c.836T>G | XP_016885036.1:p.Ile279Ser | |
| XM_017029548.1:c.836T>G | XP_016885037.1:p.Ile279Ser | |
| XM_017029549.1:c.791T>G | XP_016885038.1:p.Ile264Ser | |
| XM_017029550.1:c.680T>G | XP_016885039.1:p.Ile227Ser | |
| XM_017029551.2:c.47T>G | XP_016885040.1:p.Ile16Ser | |
| NM_000252.3:c.791T>G MANE Select | NP_000243.1:p.Ile264Ser | |
| NM_001376906.1:c.791T>G | NP_001363835.1:p.Ile264Ser | |
| NM_001376907.1:c.680T>G | NP_001363836.1:p.Ile227Ser | |
| NM_001376908.1:c.791T>G | NP_001363837.1:p.Ile264Ser |