Linked Data
ClinVar Variation Id:
194770
dbSNP Id:
rs368535131
ExAC:
17:56283726 C / T
gnomAD v2:
17-56283726-C-T
gnomAD v3:
17-58206365-C-T
gnomAD v4:
17-58206365-C-T
COSMIC:
COSM3388040
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58206365C>T , CM000679.2:g.58206365C>T | GRCh38 |
| NC_000017.10:g.56283726C>T , CM000679.1:g.56283726C>T | GRCh37 |
| NC_000017.9:g.53638725C>T | NCBI36 |
| NG_013020.1:g.18638C>T | |
| NG_013032.1:g.18241G>A , LRG_687:g.18241G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313863.11:c.1289G>A | ENSP00000316631.6:p.Arg430Gln | |
| ENST00000393119.7:c.1506G>A MANE Select | ENSP00000376827.2:p.Ser502= | |
| ENST00000537529.7:c.1077G>A | ENSP00000442096.3:p.Ser359= | |
| ENST00000675753.2:c.*1125G>A | ENSP00000502156.1:n.*1125G>A | |
| ENST00000676787.1:c.1377G>A | ENSP00000503999.1:p.Ser459= | |
| ENST00000677111.1:c.*980G>A | ENSP00000504282.1:n.*980G>A | |
| ENST00000677160.1:n.2780G>A | ||
| ENST00000677416.1:n.2827G>A | ||
| ENST00000677486.1:c.*850G>A | ENSP00000503852.1:n.*850G>A | |
| ENST00000677709.1:n.2206G>A | ||
| ENST00000678011.1:n.2406G>A | ||
| ENST00000678432.1:c.*1280G>A | ENSP00000504452.1:n.*1280G>A | |
| ENST00000678463.1:c.1423G>A | ENSP00000502984.1:p.Glu475Lys | |
| ENST00000678568.1:c.*830G>A | ENSP00000504754.1:n.*830G>A | |
| ENST00000678641.1:c.*850G>A | ENSP00000503159.1:n.*850G>A | |
| ENST00000678763.1:n.1821G>A | ||
| ENST00000313863.10:c.1289G>A | ENSP00000316631.6:p.Arg430Gln | |
| ENST00000393119.6:c.1506G>A | ENSP00000376827.2:p.Ser502= | |
| ENST00000393120.6:c.*913G>A | ENSP00000376828.2:n.*913G>A | |
| ENST00000537529.6:c.1476G>A | ENSP00000442096.2:p.Ser492= | |
| ENST00000583577.1:n.332G>A | ||
| NM_001165927.1:c.1476G>A , LRG_687t2:c.1476G>A | NP_001159399.1:p.Ser492= | |
| NM_017777.3:c.1506G>A , LRG_687t1:c.1506G>A | NP_060247.2:p.Ser502= | |
| XM_005257483.3:c.1423G>A | XP_005257540.1:p.Glu475Lys | |
| XM_005257485.3:c.994G>A | XP_005257542.1:p.Glu332Lys | |
| XM_005257486.3:c.897G>A | XP_005257543.1:p.Ser299= | |
| XM_006721965.2:c.814G>A | XP_006722028.1:p.Glu272Lys | |
| XM_011524957.1:c.1432G>A | XP_011523259.1:p.Glu478Lys | |
| XM_011524958.1:c.1515G>A | XP_011523260.1:p.Ser505= | |
| XM_011524959.1:c.1298G>A | XP_011523261.1:p.Arg433Gln | |
| NM_001321268.1:c.897G>A | NP_001308197.1:p.Ser299= | |
| NM_001321269.1:c.1423G>A | NP_001308198.1:p.Glu475Lys | |
| NM_001330397.1:c.1289G>A | NP_001317326.1:p.Arg430Gln | |
| XM_005257485.4:c.994G>A | XP_005257542.1:p.Glu332Lys | |
| XM_006721965.3:c.814G>A | XP_006722028.1:p.Glu272Lys | |
| XM_011524957.2:c.1432G>A | XP_011523259.1:p.Glu478Lys | |
| XM_011524958.2:c.1515G>A | XP_011523260.1:p.Ser505= | |
| XM_011524959.2:c.1298G>A | XP_011523261.1:p.Arg433Gln | |
| XM_017024805.1:c.1077G>A | XP_016880294.1:p.Ser359= | |
| XR_002958042.1:n.1434G>A | ||
| NM_001321268.2:c.897G>A | NP_001308197.1:p.Ser299= | |
| NM_001321269.2:c.1423G>A | NP_001308198.1:p.Glu475Lys | |
| NM_001330397.2:c.1289G>A | NP_001317326.1:p.Arg430Gln | |
| NM_017777.4:c.1506G>A MANE Select | NP_060247.2:p.Ser502= |