Revel Score:
ENST00000487664
0.552
ENST00000298480
0.552
ENST00000371757 (MANE Select)
0.552
ENST00000486577
0.552
ENST00000491806
0.552
ENST00000488444
0.552
ENST00000490355
0.552
ENST00000263604
0.552
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.135779429G>T , CM000671.2:g.135779429G>T | GRCh38 |
| NC_000009.11:g.138671275G>T , CM000671.1:g.138671275G>T | GRCh37 |
| NC_000009.10:g.137811096G>T | NCBI36 |
| NG_033070.1:g.82245G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371757.7:c.2800G>T MANE Select | ENSP00000360822.2:p.Ala934Ser | |
| ENST00000674572.1:c.2641G>T | ENSP00000501742.1:p.Ala881Ser | |
| ENST00000675090.1:c.2548G>T | ENSP00000501833.1:p.Ala850Ser | |
| ENST00000675102.1:n.1334G>T | ||
| ENST00000675399.1:c.2548G>T | ENSP00000501932.1:p.Ala850Ser | |
| ENST00000676421.1:c.2557G>T | ENSP00000502322.1:p.Ala853Ser | |
| ENST00000263604.5:c.2701G>T | ENSP00000263604.4:p.Ala901Ser | |
| ENST00000371757.6:c.2800G>T | ENSP00000360822.2:p.Ala934Ser | |
| ENST00000460750.5:c.*2410G>T | ENSP00000418777.1:n.*2410G>T | |
| ENST00000486577.6:c.2683G>T | ENSP00000417578.3:p.Ala895Ser | |
| ENST00000487664.5:c.2800G>T | ENSP00000417851.2:p.Ala934Ser | |
| ENST00000488444.6:c.2743G>T | ENSP00000419007.3:p.Ala915Ser | |
| ENST00000490355.6:c.2737G>T | ENSP00000418003.3:p.Ala913Ser | |
| ENST00000490363.3:n.2619G>T | ||
| ENST00000491806.6:c.2743G>T | ENSP00000419086.3:p.Ala915Ser | |
| ENST00000628528.2:c.2665G>T | ENSP00000486374.1:p.Ala889Ser | |
| ENST00000630792.2:c.2635G>T | ENSP00000486486.1:p.Ala879Ser | |
| ENST00000631073.2:c.2743G>T | ENSP00000486130.1:p.Ala915Ser | |
| ENST00000631193.1:c.666G>T | ENSP00000486830.1:n.666G>T | |
| NM_001272003.1:c.2665G>T | NP_001258932.1:p.Ala889Ser | |
| NM_020822.2:c.2800G>T | NP_065873.2:p.Ala934Ser | |
| XM_011518877.1:c.2935G>T | XP_011517179.1:p.Ala979Ser | |
| XM_011518878.1:c.2944G>T | XP_011517180.1:p.Ala982Ser | |
| XM_011518879.1:c.2935G>T | XP_011517181.1:p.Ala979Ser | |
| XM_011518880.1:c.2701G>T | XP_011517182.1:p.Ala901Ser | |
| XM_011518881.1:c.2290G>T | XP_011517183.1:p.Ala764Ser | |
| XM_011518877.3:c.2935G>T | XP_011517179.1:p.Ala979Ser | |
| XM_011518878.3:c.2944G>T | XP_011517180.1:p.Ala982Ser | |
| XM_011518879.3:c.2935G>T | XP_011517181.1:p.Ala979Ser | |
| XM_011518881.3:c.2290G>T | XP_011517183.1:p.Ala764Ser | |
| XM_017014931.1:c.2734G>T | XP_016870420.1:p.Ala912Ser | |
| XM_017014932.1:c.2557G>T | XP_016870421.1:p.Ala853Ser | |
| XM_017014933.1:c.2290G>T | XP_016870422.1:p.Ala764Ser | |
| XM_024447617.1:c.2290G>T | XP_024303385.1:p.Ala764Ser | |
| XM_024447618.1:c.2290G>T | XP_024303386.1:p.Ala764Ser | |
| NM_020822.3:c.2800G>T MANE Select | NP_065873.2:p.Ala934Ser | |
| NM_001272003.2:c.2665G>T | NP_001258932.1:p.Ala889Ser |