Revel Score:
ENST00000423058
0.907
ENST00000303395
0.907
ENST00000375405
0.907
ENST00000409050
0.907
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.166002647G>A , CM000664.2:g.166002647G>A | GRCh38 |
| NC_000002.11:g.166859157G>A , CM000664.1:g.166859157G>A | GRCh37 |
| NC_000002.10:g.166567403G>A | NCBI36 |
| NG_011906.1:g.75993C>T , LRG_8:g.75993C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689288.1:c.*2145C>T | ENSP00000509637.1:n.*2145C>T | |
| ENST00000303395.9:c.4109C>T | ENSP00000303540.4:p.Ala1370Val | |
| ENST00000635750.1:c.4076C>T | ENSP00000490799.1:p.Ala1359Val | |
| ENST00000635776.1:c.4076C>T | ENSP00000490692.1:p.Ala1359Val | |
| ENST00000636194.1:c.*1602C>T | ENSP00000490288.1:n.*1602C>T | |
| ENST00000637038.1:c.971C>T | ||
| ENST00000637988.1:c.4076C>T | ENSP00000490780.1:p.Ala1359Val | |
| ENST00000640036.1:c.4076C>T | ENSP00000491573.1:p.Ala1359Val | |
| ENST00000641575.1:c.4073C>T | ENSP00000492917.1:p.Ala1358Val | |
| ENST00000641603.1:c.4003-2871C>T | ENSP00000492945.1:n.4003-2871C>T | |
| ENST00000641996.1:c.*3663C>T | ENSP00000493054.1:n.*3663C>T | |
| ENST00000671940.1:c.*2052C>T | ENSP00000500336.1:n.*2052C>T | |
| ENST00000673490.1:n.6582C>T | ||
| ENST00000674923.1:c.4109C>T MANE Select | ENSP00000501589.1:p.Ala1370Val | |
| ENST00000303395.8:c.4109C>T | ENSP00000303540.4:p.Ala1370Val | |
| ENST00000375405.7:c.4076C>T | ENSP00000364554.3:p.Ala1359Val | |
| ENST00000409050.1:c.4025C>T | ENSP00000386312.1:p.Ala1342Val | |
| ENST00000423058.6:c.4109C>T | ENSP00000407030.2:p.Ala1370Val | |
| ENST00000491429.1:n.262C>T | ||
| NM_001165963.1:c.4109C>T | NP_001159435.1:p.Ala1370Val | |
| NM_001165964.1:c.4025C>T | NP_001159436.1:p.Ala1342Val | |
| NM_001202435.1:c.4109C>T | NP_001189364.1:p.Ala1370Val | |
| NM_006920.4:c.4076C>T , LRG_8t1:c.4076C>T | NP_008851.3:p.Ala1359Val | |
| NR_110598.1:n.176-12966G>A | ||
| XM_011511598.1:c.4109C>T | XP_011509900.1:p.Ala1370Val | |
| XM_011511599.1:c.4109C>T | XP_011509901.1:p.Ala1370Val | |
| XM_011511600.1:c.4109C>T | XP_011509902.1:p.Ala1370Val | |
| XM_011511601.1:c.4109C>T | XP_011509903.1:p.Ala1370Val | |
| XM_011511602.1:c.4109C>T | XP_011509904.1:p.Ala1370Val | |
| XM_011511603.1:c.4106C>T | XP_011509905.1:p.Ala1369Val | |
| XM_011511604.1:c.4076C>T | XP_011509906.1:p.Ala1359Val | |
| XM_011511605.1:c.4073C>T | XP_011509907.1:p.Ala1358Val | |
| XM_011511606.1:c.4025C>T | XP_011509908.1:p.Ala1342Val | |
| XM_011511607.1:c.4003-2871C>T | XP_011509909.1:n.4003-2871C>T | |
| XR_922981.1:n.4357C>T | ||
| NM_001165963.2:c.4109C>T | NP_001159435.1:p.Ala1370Val | |
| NM_001165964.2:c.4025C>T | NP_001159436.1:p.Ala1342Val | |
| NM_001202435.2:c.4109C>T | NP_001189364.1:p.Ala1370Val | |
| NM_001353948.1:c.4109C>T | NP_001340877.1:p.Ala1370Val | |
| NM_001353949.1:c.4076C>T | NP_001340878.1:p.Ala1359Val | |
| NM_001353950.1:c.4076C>T | NP_001340879.1:p.Ala1359Val | |
| NM_001353951.1:c.4076C>T | NP_001340880.1:p.Ala1359Val | |
| NM_001353952.1:c.4076C>T | NP_001340881.1:p.Ala1359Val | |
| NM_001353954.1:c.4073C>T | NP_001340883.1:p.Ala1358Val | |
| NM_001353955.1:c.4073C>T | NP_001340884.1:p.Ala1358Val | |
| NM_001353957.1:c.4025C>T | NP_001340886.1:p.Ala1342Val | |
| NM_001353958.1:c.4025C>T | NP_001340887.1:p.Ala1342Val | |
| NM_001353960.1:c.4022C>T | NP_001340889.1:p.Ala1341Val | |
| NM_001353961.1:c.1667C>T | NP_001340890.1:p.Ala556Val | |
| NM_006920.5:c.4076C>T | NP_008851.3:p.Ala1359Val | |
| NR_148667.1:n.4545C>T | ||
| XR_001738883.1:n.4559C>T | ||
| XR_001738884.1:n.4531C>T | ||
| NM_001165963.3:c.4109C>T | NP_001159435.1:p.Ala1370Val | |
| NM_001165964.3:c.4025C>T | NP_001159436.1:p.Ala1342Val | |
| NM_001202435.3:c.4109C>T | NP_001189364.1:p.Ala1370Val | |
| NM_001353948.2:c.4109C>T | NP_001340877.1:p.Ala1370Val | |
| NM_001353949.2:c.4076C>T | NP_001340878.1:p.Ala1359Val | |
| NM_001353950.2:c.4076C>T | NP_001340879.1:p.Ala1359Val | |
| NM_001353951.2:c.4076C>T | NP_001340880.1:p.Ala1359Val | |
| NM_001353952.2:c.4076C>T | NP_001340881.1:p.Ala1359Val | |
| NM_001353954.2:c.4073C>T | NP_001340883.1:p.Ala1358Val | |
| NM_001353955.2:c.4073C>T | NP_001340884.1:p.Ala1358Val | |
| NM_001353957.2:c.4025C>T | NP_001340886.1:p.Ala1342Val | |
| NM_001353958.2:c.4025C>T | NP_001340887.1:p.Ala1342Val | |
| NM_001353960.2:c.4022C>T | NP_001340889.1:p.Ala1341Val | |
| NM_001353961.2:c.1667C>T | NP_001340890.1:p.Ala556Val | |
| NM_006920.6:c.4076C>T | NP_008851.3:p.Ala1359Val | |
| NR_148667.2:n.4526C>T | ||
| NM_001165963.4:c.4109C>T MANE Select | NP_001159435.1:p.Ala1370Val |