Linked Data
ClinVar Variation Id:
260878
dbSNP Id:
rs201998680
ExAC:
17:56288030 C / T
gnomAD v2:
17-56288030-C-T
gnomAD v3:
17-58210669-C-T
gnomAD v4:
17-58210669-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58210669C>T , CM000679.2:g.58210669C>T | GRCh38 |
| NC_000017.10:g.56288030C>T , CM000679.1:g.56288030C>T | GRCh37 |
| NC_000017.9:g.53643029C>T | NCBI36 |
| NG_013032.1:g.13937G>A , LRG_687:g.13937G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313863.11:c.1014G>A | ENSP00000316631.6:p.Leu338= | |
| ENST00000393119.7:c.1014G>A MANE Select | ENSP00000376827.2:p.Leu338= | |
| ENST00000537529.7:c.585G>A | ENSP00000442096.3:p.Leu195= | |
| ENST00000580127.6:c.1014G>A | ENSP00000462423.2:p.Leu338= | |
| ENST00000581761.6:c.1014G>A | ENSP00000462129.2:p.Leu338= | |
| ENST00000585134.2:c.1014G>A | ENSP00000463826.2:p.Leu338= | |
| ENST00000675753.2:c.*633G>A | ENSP00000502156.1:n.*633G>A | |
| ENST00000676787.1:c.885G>A | ENSP00000503999.1:p.Leu295= | |
| ENST00000677111.1:c.915+1709G>A | ENSP00000504282.1:n.915+1709G>A | |
| ENST00000677160.1:n.2288G>A | ||
| ENST00000677416.1:n.1039G>A | ||
| ENST00000677486.1:c.*358G>A | ENSP00000503852.1:n.*358G>A | |
| ENST00000677546.1:c.*315G>A | ENSP00000504043.1:n.*315G>A | |
| ENST00000677709.1:n.1039G>A | ||
| ENST00000678011.1:n.1039G>A | ||
| ENST00000678432.1:c.*633G>A | ENSP00000504452.1:n.*633G>A | |
| ENST00000678463.1:c.1014G>A | ENSP00000502984.1:p.Leu338= | |
| ENST00000678568.1:c.*421G>A | ENSP00000504754.1:n.*421G>A | |
| ENST00000678641.1:c.*358G>A | ENSP00000503159.1:n.*358G>A | |
| ENST00000678763.1:n.792G>A | ||
| ENST00000313863.10:c.1014G>A | ENSP00000316631.6:p.Leu338= | |
| ENST00000393119.6:c.1014G>A | ENSP00000376827.2:p.Leu338= | |
| ENST00000393120.6:c.*421G>A | ENSP00000376828.2:n.*421G>A | |
| ENST00000537529.6:c.984G>A | ENSP00000442096.2:p.Leu328= | |
| ENST00000577315.5:c.67G>A | ||
| ENST00000577824.5:c.491G>A | ||
| ENST00000579358.1:n.452G>A | ||
| ENST00000581761.5:c.*421G>A | ENSP00000462129.1:n.*421G>A | |
| ENST00000585134.1:c.237G>A | ENSP00000463826.1:p.Leu79= | |
| NM_001165927.1:c.984G>A , LRG_687t2:c.984G>A | NP_001159399.1:p.Leu328= | |
| NM_017777.3:c.1014G>A , LRG_687t1:c.1014G>A | NP_060247.2:p.Leu338= | |
| XM_005257483.3:c.1014G>A | XP_005257540.1:p.Leu338= | |
| XM_005257485.3:c.585G>A | XP_005257542.1:p.Leu195= | |
| XM_005257486.3:c.405G>A | XP_005257543.1:p.Leu135= | |
| XM_006721965.2:c.405G>A | XP_006722028.1:p.Leu135= | |
| XM_011524957.1:c.1023G>A | XP_011523259.1:p.Leu341= | |
| XM_011524958.1:c.1023G>A | XP_011523260.1:p.Leu341= | |
| XM_011524959.1:c.1023G>A | XP_011523261.1:p.Leu341= | |
| XM_011524960.1:c.1023G>A | XP_011523262.1:p.Leu341= | |
| XR_934494.1:n.1028G>A | ||
| NM_001321268.1:c.405G>A | NP_001308197.1:p.Leu135= | |
| NM_001321269.1:c.1014G>A | NP_001308198.1:p.Leu338= | |
| NM_001330397.1:c.1014G>A | NP_001317326.1:p.Leu338= | |
| XM_005257485.4:c.585G>A | XP_005257542.1:p.Leu195= | |
| XM_006721965.3:c.405G>A | XP_006722028.1:p.Leu135= | |
| XM_011524957.2:c.1023G>A | XP_011523259.1:p.Leu341= | |
| XM_011524958.2:c.1023G>A | XP_011523260.1:p.Leu341= | |
| XM_011524959.2:c.1023G>A | XP_011523261.1:p.Leu341= | |
| XM_011524960.2:c.1023G>A | XP_011523262.1:p.Leu341= | |
| XM_017024804.2:c.1014G>A | XP_016880293.1:p.Leu338= | |
| XM_017024805.1:c.585G>A | XP_016880294.1:p.Leu195= | |
| XR_002958042.1:n.1025G>A | ||
| NM_001321268.2:c.405G>A | NP_001308197.1:p.Leu135= | |
| NM_001321269.2:c.1014G>A | NP_001308198.1:p.Leu338= | |
| NM_001330397.2:c.1014G>A | NP_001317326.1:p.Leu338= | |
| NM_017777.4:c.1014G>A MANE Select | NP_060247.2:p.Leu338= |