ClinVar RCV:
ClinVar Variation:
dbSNP:
Revel Score:
ENST00000218099 (MANE Select)
0.678
ENST00000394090
0.678
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.139551251A>T , CM000685.2:g.139551251A>T | GRCh38 |
| NC_000023.10:g.138633410A>T , CM000685.1:g.138633410A>T | GRCh37 |
| NC_000023.9:g.138461076A>T | NCBI36 |
| NG_007994.1:g.25516A>T , LRG_556:g.25516A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218099.7:c.710A>T MANE Select | ENSP00000218099.2:p.Gln237Leu | |
| ENST00000643157.1:n.1377A>T | ||
| ENST00000218099.6:c.710A>T | ENSP00000218099.2:p.Gln237Leu | |
| ENST00000394090.2:c.596A>T | ENSP00000377650.2:p.Gln199Leu | |
| NM_000133.3:c.710A>T , LRG_556t1:c.710A>T | NP_000124.1:p.Gln237Leu | |
| NM_001313913.1:c.596A>T | NP_001300842.1:p.Gln199Leu | |
| XM_005262397.3:c.581A>T | XP_005262454.1:p.Gln194Leu | |
| XM_005262397.4:c.581A>T | XP_005262454.1:p.Gln194Leu | |
| NM_000133.4:c.710A>T MANE Select | NP_000124.1:p.Gln237Leu | |
| NM_001313913.2:c.596A>T | NP_001300842.1:p.Gln199Leu |