Revel Score:
ENST00000231790 (MANE Select)
0.954
ENST00000383761
0.954
ENST00000421440
0.954
ENST00000458205
0.954
ENST00000539477
0.954
ENST00000455445
0.954
ENST00000435176
0.954
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.37050648T>C , CM000665.2:g.37050648T>C | GRCh38 |
| NC_000003.11:g.37092139T>C , CM000665.1:g.37092139T>C | GRCh37 |
| NC_000003.10:g.37067143T>C | NCBI36 |
| NG_007109.2:g.62299T>C , LRG_216:g.62299T>C | |
| NG_053016.1:g.131170A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000413740.2:c.1830T>C | ENSP00000416476.2:p.Gly610= | |
| ENST00000429117.6:c.1972T>C | ENSP00000407019.2:p.Cys658Arg | |
| ENST00000456676.7:c.2059T>C | ENSP00000416687.3:p.Cys687Arg | |
| ENST00000492474.6:c.1543T>C | ENSP00000518393.1:p.Cys515Arg | |
| ENST00000616768.6:c.2173T>C | ENSP00000480669.3:p.Cys725Arg | |
| ENST00000673673.2:c.2101T>C | ENSP00000500979.2:p.Cys701Arg | |
| ENST00000231790.8:c.2266T>C MANE Select | ENSP00000231790.3:p.Cys756Arg | |
| ENST00000413212.2:c.*1184T>C | ENSP00000400844.2:n.*1184T>C | |
| ENST00000432299.6:c.*2098T>C | ENSP00000416783.1:n.*2098T>C | |
| ENST00000447829.6:c.*1377T>C | ENSP00000399329.2:n.*1377T>C | |
| ENST00000539477.6:c.1543T>C | ENSP00000443665.1:p.Cys515Arg | |
| ENST00000616768.5:c.1210T>C | ENSP00000480669.2:p.Cys404Arg | |
| ENST00000673673.1:c.2054T>C | ||
| ENST00000673741.1:n.1300T>C | ||
| ENST00000673889.1:n.1648T>C | ||
| ENST00000673897.1:c.*2058T>C | ENSP00000501109.1:n.*2058T>C | |
| ENST00000673899.1:c.1534T>C | ENSP00000501030.1:p.Cys512Arg | |
| ENST00000673947.1:c.*2406T>C | ENSP00000501304.1:n.*2406T>C | |
| ENST00000673972.1:c.*2144T>C | ENSP00000501281.1:n.*2144T>C | |
| ENST00000674019.1:c.1543T>C | ENSP00000501081.1:p.Cys515Arg | |
| ENST00000674111.1:c.*495T>C | ENSP00000501162.1:n.*495T>C | |
| ENST00000674125.1:n.977T>C | ||
| ENST00000231790.6:c.2266T>C | ENSP00000231790.2:p.Cys756Arg | |
| ENST00000435176.5:c.1972T>C | ENSP00000402564.1:p.Cys658Arg | |
| ENST00000455445.6:c.1543T>C | ENSP00000398272.2:p.Cys515Arg | |
| ENST00000456676.6:c.2034T>C | ||
| ENST00000458205.6:c.1543T>C | ENSP00000402667.2:p.Cys515Arg | |
| ENST00000536378.5:c.1543T>C | ENSP00000444286.2:p.Cys515Arg | |
| ENST00000539477.5:c.1543T>C | ENSP00000443665.1:p.Cys515Arg | |
| NM_000249.3:c.2266T>C , LRG_216t1:c.2266T>C | NP_000240.1:p.Cys756Arg | |
| NM_001167617.1:c.1972T>C | NP_001161089.1:p.Cys658Arg | |
| NM_001167618.1:c.1543T>C | NP_001161090.1:p.Cys515Arg | |
| NM_001167619.1:c.1543T>C | NP_001161091.1:p.Cys515Arg | |
| NM_001258271.1:c.2059T>C | NP_001245200.1:p.Cys687Arg | |
| NM_001258273.1:c.1543T>C | NP_001245202.1:p.Cys515Arg | |
| NM_001258274.1:c.1543T>C | NP_001245203.1:p.Cys515Arg | |
| XM_005265161.1:c.2059T>C | XP_005265218.1:p.Cys687Arg | |
| XM_005265163.1:c.1543T>C | XP_005265220.1:p.Cys515Arg | |
| XM_005265164.1:c.1543T>C | XP_005265221.1:p.Cys515Arg | |
| XM_005265166.1:c.1243T>C | XP_005265223.1:p.Cys415Arg | |
| XM_011533727.1:c.1192T>C | XP_011532029.1:p.Cys398Arg | |
| NM_001167617.2:c.1972T>C | NP_001161089.1:p.Cys658Arg | |
| NM_001167618.2:c.1543T>C | NP_001161090.1:p.Cys515Arg | |
| NM_001167619.2:c.1543T>C | NP_001161091.1:p.Cys515Arg | |
| NM_001258274.2:c.1543T>C | NP_001245203.1:p.Cys515Arg | |
| NM_001354615.1:c.1543T>C | NP_001341544.1:p.Cys515Arg | |
| NM_001354616.1:c.1543T>C | NP_001341545.1:p.Cys515Arg | |
| NM_001354617.1:c.1543T>C | NP_001341546.1:p.Cys515Arg | |
| NM_001354618.1:c.1543T>C | NP_001341547.1:p.Cys515Arg | |
| NM_001354619.1:c.1543T>C | NP_001341548.1:p.Cys515Arg | |
| NM_001354620.1:c.1972T>C | NP_001341549.1:p.Cys658Arg | |
| NM_001354621.1:c.1243T>C | NP_001341550.1:p.Cys415Arg | |
| NM_001354622.1:c.1243T>C | NP_001341551.1:p.Cys415Arg | |
| NM_001354623.1:c.1243T>C | NP_001341552.1:p.Cys415Arg | |
| NM_001354624.1:c.1192T>C | NP_001341553.1:p.Cys398Arg | |
| NM_001354625.1:c.1192T>C | NP_001341554.1:p.Cys398Arg | |
| NM_001354626.1:c.1192T>C | NP_001341555.1:p.Cys398Arg | |
| NM_001354627.1:c.1192T>C | NP_001341556.1:p.Cys398Arg | |
| NM_001354628.1:c.2173T>C | NP_001341557.1:p.Cys725Arg | |
| NM_001354629.1:c.2167T>C | NP_001341558.1:p.Cys723Arg | |
| NM_001354630.1:c.2101T>C | NP_001341559.1:p.Cys701Arg | |
| XM_005265161.2:c.2059T>C | XP_005265218.1:p.Cys687Arg | |
| XM_017006450.2:c.1243T>C | XP_016861939.1:p.Cys415Arg | |
| NM_000249.4:c.2266T>C MANE Select | NP_000240.1:p.Cys756Arg | |
| NM_001167617.3:c.1972T>C | NP_001161089.1:p.Cys658Arg | |
| NM_001167618.3:c.1543T>C | NP_001161090.1:p.Cys515Arg | |
| NM_001167619.3:c.1543T>C | NP_001161091.1:p.Cys515Arg | |
| NM_001258271.2:c.2059T>C | NP_001245200.1:p.Cys687Arg | |
| NM_001258273.2:c.1543T>C | NP_001245202.1:p.Cys515Arg | |
| NM_001258274.3:c.1543T>C | NP_001245203.1:p.Cys515Arg | |
| NM_001354615.2:c.1543T>C | NP_001341544.1:p.Cys515Arg | |
| NM_001354616.2:c.1543T>C | NP_001341545.1:p.Cys515Arg | |
| NM_001354617.2:c.1543T>C | NP_001341546.1:p.Cys515Arg | |
| NM_001354618.2:c.1543T>C | NP_001341547.1:p.Cys515Arg | |
| NM_001354619.2:c.1543T>C | NP_001341548.1:p.Cys515Arg | |
| NM_001354620.2:c.1972T>C | NP_001341549.1:p.Cys658Arg | |
| NM_001354621.2:c.1243T>C | NP_001341550.1:p.Cys415Arg | |
| NM_001354622.2:c.1243T>C | NP_001341551.1:p.Cys415Arg | |
| NM_001354623.2:c.1243T>C | NP_001341552.1:p.Cys415Arg | |
| NM_001354624.2:c.1192T>C | NP_001341553.1:p.Cys398Arg | |
| NM_001354625.2:c.1192T>C | NP_001341554.1:p.Cys398Arg | |
| NM_001354626.2:c.1192T>C | NP_001341555.1:p.Cys398Arg | |
| NM_001354627.2:c.1192T>C | NP_001341556.1:p.Cys398Arg | |
| NM_001354628.2:c.2173T>C | NP_001341557.1:p.Cys725Arg | |
| NM_001354629.2:c.2167T>C | NP_001341558.1:p.Cys723Arg | |
| NM_001354630.2:c.2101T>C | NP_001341559.1:p.Cys701Arg |