Linked Data
ClinVar Variation Id:
299314
dbSNP Id:
rs114767681
ExAC:
10:14950995 A / G
gnomAD v2:
10-14950995-A-G
gnomAD v3:
10-14908996-A-G
gnomAD v4:
10-14908996-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.14908996A>G , CM000672.2:g.14908996A>G | GRCh38 |
| NC_000010.10:g.14950995A>G , CM000672.1:g.14950995A>G | GRCh37 |
| NC_000010.9:g.14991001A>G | NCBI36 |
| NG_007276.1:g.50100T>C , LRG_54:g.50100T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000378241.6:c.*1679T>C | ENSP00000367487.3:n.*1679T>C | |
| ENST00000456122.2:c.*1343-9684T>C | ENSP00000413180.3:n.*1343-9684T>C | |
| ENST00000489161.2:c.*1214T>C | ENSP00000513000.2:n.*1214T>C | |
| ENST00000492201.6:c.*485T>C | ENSP00000512999.1:n.*485T>C | |
| ENST00000697047.1:c.1491T>C | ENSP00000513066.1:p.Asp497= | |
| ENST00000697070.1:c.1491T>C | ENSP00000513085.1:p.Asp497= | |
| ENST00000697071.1:c.*1411T>C | ENSP00000513086.1:n.*1411T>C | |
| ENST00000697072.1:c.*503T>C | ENSP00000513087.1:n.*503T>C | |
| ENST00000697073.1:c.*1269T>C | ENSP00000513088.2:n.*1269T>C | |
| ENST00000697074.1:c.*1269T>C | ENSP00000513089.2:n.*1269T>C | |
| ENST00000697075.1:c.1491T>C | ENSP00000513090.1:p.Asp497= | |
| ENST00000697076.1:c.*503T>C | ENSP00000513091.1:n.*503T>C | |
| ENST00000697077.1:c.*1202T>C | ENSP00000513092.1:n.*1202T>C | |
| ENST00000697078.1:c.*1198T>C | ENSP00000513093.1:n.*1198T>C | |
| ENST00000697079.1:n.1195T>C | ||
| ENST00000697080.1:c.*1355T>C | ENSP00000513094.1:n.*1355T>C | |
| ENST00000697081.1:c.*1249T>C | ENSP00000513095.1:n.*1249T>C | |
| ENST00000697082.1:c.*1520T>C | ENSP00000513096.1:n.*1520T>C | |
| ENST00000697083.1:c.*1296T>C | ENSP00000513097.1:n.*1296T>C | |
| ENST00000697084.1:c.1548T>C | ENSP00000513098.1:p.Asp516= | |
| ENST00000697085.1:c.*1258T>C | ENSP00000513099.1:n.*1258T>C | |
| ENST00000697086.1:n.4067T>C | ||
| ENST00000378278.7:c.1491T>C MANE Select | ENSP00000367527.2:p.Asp497= | |
| ENST00000357717.6:c.1146T>C | ENSP00000350349.2:p.Asp382= | |
| ENST00000378242.1:c.450T>C | ENSP00000367488.1:p.Asp150= | |
| ENST00000378246.6:c.1146T>C | ENSP00000367492.2:p.Asp382= | |
| ENST00000378249.5:c.1146T>C | ENSP00000367496.1:p.Asp382= | |
| ENST00000378254.5:c.1131T>C | ENSP00000367502.1:p.Asp377= | |
| ENST00000378255.5:c.1131T>C | ENSP00000367503.1:p.Asp377= | |
| ENST00000378258.5:c.1131T>C | ENSP00000367506.1:p.Asp377= | |
| ENST00000378278.6:c.1491T>C | ENSP00000367527.2:p.Asp497= | |
| ENST00000378289.8:c.1157-9684T>C | ENSP00000367538.4:n.1157-9684T>C | |
| ENST00000396817.6:c.1131T>C | ENSP00000380030.2:p.Asp377= | |
| ENST00000492201.5:n.706T>C | ||
| NM_001033855.2:c.1491T>C | NP_001029027.1:p.Asp497= | |
| NM_001033857.2:c.1131T>C | NP_001029029.1:p.Asp377= | |
| NM_001033858.2:c.1131T>C | NP_001029030.1:p.Asp377= | |
| NM_001289076.1:c.1146T>C | NP_001276005.1:p.Asp382= | |
| NM_001289077.1:c.1131T>C | NP_001276006.1:p.Asp377= | |
| NM_001289078.1:c.1146T>C | NP_001276007.1:p.Asp382= | |
| NM_001289079.1:c.1131T>C | NP_001276008.1:p.Asp377= | |
| NM_022487.3:c.1146T>C | NP_071932.2:p.Asp382= | |
| NR_110297.1:n.2266T>C | ||
| XM_006717491.2:c.1146T>C | XP_006717554.1:p.Asp382= | |
| XM_011519616.1:c.1146T>C | XP_011517918.1:p.Asp382= | |
| XM_011519617.1:c.1146T>C | XP_011517919.1:p.Asp382= | |
| XM_011519618.1:c.1146T>C | XP_011517920.1:p.Asp382= | |
| XM_011519619.1:c.1131T>C | XP_011517921.1:p.Asp377= | |
| NM_001350965.1:c.1491T>C | NP_001337894.1:p.Asp497= | |
| NM_001350966.1:c.1146T>C | NP_001337895.1:p.Asp382= | |
| NM_001350967.1:c.1131T>C | NP_001337896.1:p.Asp377= | |
| NR_146960.1:n.1858T>C | ||
| NR_146961.1:n.2007T>C | ||
| NR_146962.1:n.1978T>C | ||
| XM_006717491.4:c.1146T>C | XP_006717554.1:p.Asp382= | |
| XM_017016557.1:c.1146T>C | XP_016872046.1:p.Asp382= | |
| XM_017016558.1:c.1131T>C | XP_016872047.1:p.Asp377= | |
| XM_024448134.1:c.1131T>C | XP_024303902.1:p.Asp377= | |
| XM_024448135.1:c.1146T>C | XP_024303903.1:p.Asp382= | |
| XR_001747185.2:n.1780T>C | ||
| XR_001747187.1:n.1612T>C | ||
| NM_001033855.3:c.1491T>C MANE Select | NP_001029027.1:p.Asp497= | |
| NM_001033857.3:c.1131T>C | NP_001029029.1:p.Asp377= | |
| NM_001033858.3:c.1131T>C | NP_001029030.1:p.Asp377= | |
| NM_001289076.2:c.1146T>C | NP_001276005.1:p.Asp382= | |
| NM_001289077.2:c.1131T>C | NP_001276006.1:p.Asp377= | |
| NM_001289078.2:c.1146T>C | NP_001276007.1:p.Asp382= | |
| NM_001289079.2:c.1131T>C | NP_001276008.1:p.Asp377= | |
| NM_001350965.2:c.1491T>C | NP_001337894.1:p.Asp497= | |
| NM_001350966.2:c.1146T>C | NP_001337895.1:p.Asp382= | |
| NM_001350967.2:c.1131T>C | NP_001337896.1:p.Asp377= | |
| NM_022487.4:c.1146T>C | NP_071932.2:p.Asp382= | |
| NR_110297.2:n.1930T>C | ||
| NR_146961.2:n.1671T>C |