Revel Score:
ENST00000262367 (MANE Select)
0.542
ENST00000543883
0.542
ENST00000382070
0.542
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.3879880T>G , CM000678.2:g.3879880T>G | GRCh38 |
| NC_000016.9:g.3929881T>G , CM000678.1:g.3929881T>G | GRCh37 |
| NC_000016.8:g.3869882T>G | NCBI36 |
| NG_009873.1:g.5241A>C | |
| NG_009873.2:g.5834A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262367.10:c.37A>C MANE Select | ENSP00000262367.5:p.Lys13Gln | |
| ENST00000262367.9:c.37A>C | ENSP00000262367.5:p.Lys13Gln | |
| ENST00000382070.7:c.37A>C | ENSP00000371502.3:p.Lys13Gln | |
| NM_001079846.1:c.37A>C | NP_001073315.1:p.Lys13Gln | |
| NM_004380.2:c.37A>C | NP_004371.2:p.Lys13Gln | |
| XM_005255124.3:c.37A>C | XP_005255181.1:p.Lys13Gln | |
| XM_005255125.3:c.37A>C | XP_005255182.1:p.Lys13Gln | |
| XM_006720848.2:c.37A>C | XP_006720911.1:p.Lys13Gln | |
| XM_011522382.1:c.37A>C | XP_011520684.1:p.Lys13Gln | |
| XM_005255124.4:c.37A>C | XP_005255181.1:p.Lys13Gln | |
| XM_005255125.4:c.37A>C | XP_005255182.1:p.Lys13Gln | |
| XM_006720848.3:c.37A>C | XP_006720911.1:p.Lys13Gln | |
| XM_011522382.3:c.37A>C | XP_011520684.1:p.Lys13Gln | |
| XM_017022944.1:c.37A>C | XP_016878433.1:p.Lys13Gln | |
| NM_004380.3:c.37A>C MANE Select | NP_004371.2:p.Lys13Gln |