Linked Data
ClinVar Variation Id:
439191
dbSNP Id:
rs63751155
COSMIC:
COSM5967448
PubMed:
PMID:25194673
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47478289C>T , CM000664.2:g.47478289C>T | GRCh38 |
| NC_000002.11:g.47705428C>T , CM000664.1:g.47705428C>T | GRCh37 |
| NC_000002.10:g.47558932C>T | NCBI36 |
| NG_007110.2:g.80166C>T , LRG_218:g.80166C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000644900.2:c.2228C>T | ENSP00000495641.2:p.Ser743Leu | |
| ENST00000233146.7:c.2228C>T MANE Select | ENSP00000233146.2:p.Ser743Leu | |
| ENST00000543555.6:c.2030C>T | ENSP00000442697.1:p.Ser677Leu | |
| ENST00000644092.1:c.*528C>T | ENSP00000496351.1:n.*528C>T | |
| ENST00000644900.1:c.81C>T | ||
| ENST00000645339.1:c.2228C>T | ENSP00000496441.1:p.Ser743Leu | |
| ENST00000645506.1:c.2228C>T | ENSP00000495455.1:p.Ser743Leu | |
| ENST00000646415.1:c.2228C>T | ENSP00000495543.1:p.Ser743Leu | |
| ENST00000233146.6:c.2228C>T | ENSP00000233146.2:p.Ser743Leu | |
| ENST00000406134.5:c.2228C>T | ENSP00000384199.1:p.Ser743Leu | |
| ENST00000543555.5:c.2030C>T | ENSP00000442697.1:p.Ser677Leu | |
| ENST00000610696.4:c.*624C>T | ENSP00000483159.1:n.*624C>T | |
| ENST00000613514.4:c.*768C>T | ENSP00000484137.1:n.*768C>T | |
| ENST00000617333.3:c.*994C>T | ENSP00000482468.1:n.*994C>T | |
| ENST00000617938.4:c.*1200C>T | ENSP00000481158.1:n.*1200C>T | |
| ENST00000621359.2:c.2228C>T | ENSP00000481416.1:p.Ser743Leu | |
| NM_000251.2:c.2228C>T , LRG_218t1:c.2228C>T | NP_000242.1:p.Ser743Leu | |
| NM_001258281.1:c.2030C>T | NP_001245210.1:p.Ser677Leu | |
| XM_005264332.2:c.2228C>T | XP_005264389.2:p.Ser743Leu | |
| XM_011532867.1:c.2228C>T | XP_011531169.1:p.Ser743Leu | |
| XR_939685.1:n.2300C>T | ||
| XM_005264332.4:c.2228C>T | XP_005264389.2:p.Ser743Leu | |
| XM_011532867.2:c.2228C>T | XP_011531169.1:p.Ser743Leu | |
| XR_001738747.2:n.2290C>T | ||
| XR_939685.2:n.2290C>T | ||
| NM_000251.3:c.2228C>T MANE Select | NP_000242.1:p.Ser743Leu |