Revel Score:
ENST00000453658
0.014
ENST00000377245 (MANE Select)
0.014
ENST00000348208
0.014
ENST00000265384
0.014
ENST00000535702
0.014
ENST00000539225
0.014
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.69228107C>G , CM000671.2:g.69228107C>G | GRCh38 |
| NC_000009.11:g.71843023C>G , CM000671.1:g.71843023C>G | GRCh37 |
| NC_000009.10:g.71032843C>G | NCBI36 |
| NG_016342.1:g.111800C>G | |
| NG_016342.2:g.132201C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000348208.9:c.1446C>G | ENSP00000345893.4:p.Asp482Glu | |
| ENST00000377245.9:c.1446C>G MANE Select | ENSP00000366453.4:p.Asp482Glu | |
| ENST00000535702.6:c.1458C>G | ENSP00000442090.1:p.Asp486Glu | |
| ENST00000539225.2:c.1539C>G | ENSP00000438262.1:p.Asp513Glu | |
| ENST00000636247.1:n.1525C>G | ||
| ENST00000636438.1:c.1623C>G | ENSP00000489860.1:p.Asp541Glu | |
| ENST00000642889.1:c.1833C>G | ENSP00000493780.1:p.Asp611Glu | |
| ENST00000643352.1:c.*1634C>G | ENSP00000496488.1:n.*1634C>G | |
| ENST00000645088.1:c.*1753C>G | ENSP00000495447.1:n.*1753C>G | |
| ENST00000647986.1:c.1377C>G | ENSP00000496877.1:p.Asp459Glu | |
| ENST00000648042.1:c.155C>G | ||
| ENST00000648087.1:n.1763C>G | ||
| ENST00000649114.1:c.1446C>G | ENSP00000497328.1:p.Asp482Glu | |
| ENST00000649134.1:c.1458C>G | ENSP00000498068.1:p.Asp486Glu | |
| ENST00000649783.1:n.1470C>G | ||
| ENST00000649943.1:c.1446C>G | ENSP00000497539.1:p.Asp482Glu | |
| ENST00000650084.1:c.1449C>G | ENSP00000497861.1:p.Asp483Glu | |
| ENST00000650333.1:c.1377C>G | ENSP00000496791.1:p.Asp459Glu | |
| ENST00000650460.1:c.719C>G | ||
| ENST00000650522.1:n.977-1077C>G | ||
| ENST00000265384.11:c.1446C>G | ENSP00000265384.7:p.Asp482Glu | |
| ENST00000348208.8:c.1446C>G | ENSP00000345893.4:p.Asp482Glu | |
| ENST00000377245.8:c.1446C>G | ENSP00000366453.4:p.Asp482Glu | |
| ENST00000453658.6:c.1377C>G | ENSP00000392178.2:p.Asp459Glu | |
| ENST00000535702.5:c.1458C>G | ENSP00000442090.1:p.Asp486Glu | |
| ENST00000539225.1:c.1539C>G | ENSP00000438262.1:p.Asp513Glu | |
| NM_001170414.2:c.1377C>G | NP_001163885.1:p.Asp459Glu | |
| NM_001170415.1:c.1458C>G | NP_001163886.1:p.Asp486Glu | |
| NM_001170416.1:c.1539C>G | NP_001163887.1:p.Asp513Glu | |
| NM_001170630.1:c.1446C>G | NP_001164101.1:p.Asp482Glu | |
| NM_004817.3:c.1446C>G | NP_004808.2:p.Asp482Glu | |
| NM_201629.3:c.1446C>G | NP_963923.1:p.Asp482Glu | |
| XM_005252314.1:c.1458C>G | XP_005252371.1:p.Asp486Glu | |
| XM_006717324.2:c.1440C>G | XP_006717387.1:p.Asp480Glu | |
| XM_011519204.1:c.1377C>G | XP_011517506.1:p.Asp459Glu | |
| XM_011519205.1:c.1377C>G | XP_011517507.1:p.Asp459Glu | |
| XM_011519206.1:c.1377C>G | XP_011517508.1:p.Asp459Glu | |
| XM_011519207.1:c.1377C>G | XP_011517509.1:p.Asp459Glu | |
| XM_011519208.1:c.1377C>G | XP_011517510.1:p.Asp459Glu | |
| XM_011519209.1:c.1377C>G | XP_011517511.1:p.Asp459Glu | |
| NM_004817.4:c.1446C>G MANE Select | NP_004808.2:p.Asp482Glu | |
| XM_005252314.2:c.1458C>G | XP_005252371.1:p.Asp486Glu | |
| XM_011519206.2:c.1377C>G | XP_011517508.1:p.Asp459Glu | |
| XM_011519207.2:c.1377C>G | XP_011517509.1:p.Asp459Glu | |
| XM_011519208.2:c.1377C>G | XP_011517510.1:p.Asp459Glu | |
| XM_011519209.2:c.1377C>G | XP_011517511.1:p.Asp459Glu | |
| XM_017015327.2:c.1446C>G | XP_016870816.1:p.Asp482Glu | |
| XM_017015328.1:c.1458C>G | XP_016870817.1:p.Asp486Glu | |
| NM_001170416.2:c.1539C>G | NP_001163887.1:p.Asp513Glu | |
| NM_001369870.1:c.1371C>G | NP_001356799.1:p.Asp457Glu | |
| NM_001369871.1:c.1377C>G | NP_001356800.1:p.Asp459Glu | |
| NM_001369872.1:c.1446C>G | NP_001356801.1:p.Asp482Glu | |
| NM_001369873.1:c.1446C>G | NP_001356802.1:p.Asp482Glu | |
| NM_001369874.1:c.1458C>G | NP_001356803.1:p.Asp486Glu | |
| NM_001369875.1:c.1458C>G | NP_001356804.1:p.Asp486Glu |