Linked Data
ClinVar Variation Id:
44818
ClinVar RCV Id:
RCV000037939
RCV000417689
RCV000434946
RCV000420107
RCV000431024
RCV000444564
RCV000425098
RCV000438200
RCV000999627
RCV003539772
dbSNP Id:
rs397507484
COSMIC:
COSM3878760
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140753333T>G , CM000669.2:g.140753333T>G | GRCh38 |
| NC_000007.13:g.140453133T>G , CM000669.1:g.140453133T>G | GRCh37 |
| NC_000007.12:g.140099602T>G | NCBI36 |
| NG_007873.3:g.176432A>C , LRG_299:g.176432A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1802A>C MANE Select | ENSP00000493543.1:p.Lys601Thr | |
| ENST00000288602.11:c.1922A>C | ENSP00000288602.7:p.Lys641Thr | |
| ENST00000479537.6:c.472A>C | ||
| ENST00000496384.7:c.1802A>C | ENSP00000419060.2:p.Lys601Thr | |
| ENST00000497784.2:c.*1252A>C | ENSP00000420119.2:n.*1252A>C | |
| ENST00000642228.1:c.*880A>C | ENSP00000493678.1:n.*880A>C | |
| ENST00000642875.1:n.1259-3915A>C | ||
| ENST00000644120.1:n.2192A>C | ||
| ENST00000644650.1:c.898A>C | ||
| ENST00000644905.1:n.2684A>C | ||
| ENST00000644969.2:c.1922A>C MANE Plus Clinical | ENSP00000496776.1:p.Lys641Thr | |
| ENST00000646730.1:c.*378A>C | ENSP00000494784.1:n.*378A>C | |
| ENST00000646891.1:c.1802A>C | ENSP00000493543.1:p.Lys601Thr | |
| ENST00000647434.1:c.738-3915A>C | ENSP00000495132.1:n.738-3915A>C | |
| ENST00000288602.10:c.1802A>C | ENSP00000288602.6:p.Lys601Thr | |
| ENST00000479537.5:c.86A>C | ENSP00000418033.1:p.Lys29Thr | |
| ENST00000496384.6:c.625A>C | ||
| ENST00000497784.1:c.1837A>C | ENSP00000420119.1:n.1837A>C | |
| NM_004333.4:c.1802A>C , LRG_299t1:c.1802A>C | NP_004324.2:p.Lys601Thr | |
| XM_005250045.1:c.1802A>C | XP_005250102.1:p.Lys601Thr | |
| XM_005250046.1:c.1802A>C | XP_005250103.1:p.Lys601Thr | |
| XM_011516529.1:c.1802A>C | XP_011514831.1:p.Lys601Thr | |
| XM_011516530.1:c.1695-3915A>C | XP_011514832.1:n.1695-3915A>C | |
| XR_242190.1:n.1810A>C | ||
| XR_927520.1:n.1810A>C | ||
| XR_927521.1:n.1810A>C | ||
| XR_927522.1:n.1703-3915A>C | ||
| XR_927523.1:n.1703-3915A>C | ||
| NM_001354609.1:c.1802A>C | NP_001341538.1:p.Lys601Thr | |
| NM_004333.5:c.1802A>C | NP_004324.2:p.Lys601Thr | |
| NR_148928.1:n.2900A>C | ||
| XM_017012558.1:c.1922A>C | XP_016868047.1:p.Lys641Thr | |
| XM_017012559.1:c.1922A>C | XP_016868048.1:p.Lys641Thr | |
| XR_001744857.1:n.1930A>C | ||
| XR_001744858.1:n.1823-3915A>C | ||
| NM_001354609.2:c.1802A>C | NP_001341538.1:p.Lys601Thr | |
| NM_001374244.1:c.1922A>C | NP_001361173.1:p.Lys641Thr | |
| NM_001374258.1:c.1922A>C MANE Plus Clinical | NP_001361187.1:p.Lys641Thr | |
| NM_004333.6:c.1802A>C MANE Select | NP_004324.2:p.Lys601Thr | |
| NM_001378467.1:c.1811A>C | NP_001365396.1:p.Lys604Thr | |
| NM_001378468.1:c.1802A>C | NP_001365397.1:p.Lys601Thr | |
| NM_001378469.1:c.1736A>C | NP_001365398.1:p.Lys579Thr | |
| NM_001378470.1:c.1700A>C | NP_001365399.1:p.Lys567Thr | |
| NM_001378471.1:c.1691A>C | NP_001365400.1:p.Lys564Thr | |
| NM_001378472.1:c.1646A>C | NP_001365401.1:p.Lys549Thr | |
| NM_001378473.1:c.1646A>C | NP_001365402.1:p.Lys549Thr | |
| NM_001378474.1:c.1802A>C | NP_001365403.1:p.Lys601Thr | |
| NM_001378475.1:c.1538A>C | NP_001365404.1:p.Lys513Thr |