Linked Data
ClinVar Variation Id:
301528
ClinVar RCV Id:
RCV000381167
dbSNP Id:
rs574338716
ExAC:
10:90768743 C / T
gnomAD v2:
10-90768743-C-T
gnomAD v4:
10-89008986-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.89008986C>T , CM000672.2:g.89008986C>T | GRCh38 |
| NC_000010.10:g.90768743C>T , CM000672.1:g.90768743C>T | GRCh37 |
| NC_000010.9:g.90758723C>T | NCBI36 |
| NG_009089.2:g.23456C>T , LRG_134:g.23456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313771.10:n.741C>T | ||
| ENST00000355740.8:c.432C>T | ENSP00000347979.3:p.Asp144= | |
| ENST00000357339.7:c.432C>T | ENSP00000349896.2:p.Asp144= | |
| ENST00000371857.8:n.642C>T | ||
| ENST00000460510.6:c.-286C>T | ENSP00000512812.1:n.-286C>T | |
| ENST00000466081.6:n.503+1149C>T | ||
| ENST00000477270.6:c.477C>T | ENSP00000512813.1:p.Asp159= | |
| ENST00000479522.6:c.197-1553C>T | ENSP00000424113.1:n.197-1553C>T | |
| ENST00000484444.6:c.197-1553C>T | ENSP00000420975.1:n.197-1553C>T | |
| ENST00000488877.6:c.334+1149C>T | ENSP00000425159.1:n.334+1149C>T | |
| ENST00000492756.7:c.334+1149C>T | ENSP00000422453.1:n.334+1149C>T | |
| ENST00000494799.6:c.-274-1553C>T | ENSP00000512834.1:n.-274-1553C>T | |
| ENST00000562983.3:c.-286C>T | ENSP00000512845.1:n.-286C>T | |
| ENST00000612663.6:c.432C>T | ENSP00000477997.3:p.Asp144= | |
| ENST00000640140.2:n.577C>T | ||
| ENST00000640681.2:n.536C>T | ||
| ENST00000696723.1:n.4065C>T | ||
| ENST00000696741.1:n.735C>T | ||
| ENST00000696742.1:n.614C>T | ||
| ENST00000696743.1:n.604C>T | ||
| ENST00000696744.1:n.471C>T | ||
| ENST00000696767.1:n.614C>T | ||
| ENST00000696768.1:c.432C>T | ENSP00000512859.1:p.Asp144= | |
| ENST00000696769.1:n.786C>T | ||
| ENST00000696770.1:n.1666C>T | ||
| ENST00000696771.1:c.-223C>T | ENSP00000512860.1:n.-223C>T | |
| ENST00000696772.1:n.598C>T | ||
| ENST00000696773.1:n.591C>T | ||
| ENST00000696774.1:n.654C>T | ||
| ENST00000696775.1:n.707C>T | ||
| ENST00000696776.1:c.525C>T | ENSP00000512861.1:p.Asp175= | |
| ENST00000696777.1:n.516+1149C>T | ||
| ENST00000696778.1:n.614C>T | ||
| ENST00000696779.1:c.197-1553C>T | ENSP00000512862.1:n.197-1553C>T | |
| ENST00000696780.1:c.525C>T | ENSP00000512863.1:p.Asp175= | |
| ENST00000696781.1:c.334+1149C>T | ENSP00000512864.1:n.334+1149C>T | |
| ENST00000696782.1:c.432C>T | ENSP00000512865.1:p.Asp144= | |
| ENST00000696992.1:n.1549C>T | ||
| ENST00000696995.1:n.614C>T | ||
| ENST00000696996.1:n.613C>T | ||
| ENST00000696997.1:c.432C>T | ENSP00000513028.1:p.Asp144= | |
| ENST00000696998.1:n.363-1553C>T | ||
| ENST00000696999.1:c.-212+1149C>T | ENSP00000513029.1:n.-212+1149C>T | |
| ENST00000697035.1:c.432C>T | ENSP00000513059.1:p.Asp144= | |
| ENST00000697036.1:c.334+1149C>T | ENSP00000513060.1:n.334+1149C>T | |
| ENST00000697037.1:n.467C>T | ||
| ENST00000697093.1:n.656C>T | ||
| ENST00000697094.1:n.571C>T | ||
| ENST00000697095.1:c.*92C>T | ENSP00000513104.1:n.*92C>T | |
| ENST00000697096.1:n.488C>T | ||
| ENST00000697097.1:c.-286C>T | ENSP00000513105.1:n.-286C>T | |
| ENST00000562983.2:n.618C>T | ||
| ENST00000690268.1:c.513C>T | ENSP00000509810.1:p.Asp171= | |
| ENST00000355740.7:c.432C>T | ENSP00000347979.3:p.Asp144= | |
| ENST00000612663.5:c.432C>T | ENSP00000477997.3:p.Asp144= | |
| ENST00000640140.1:n.604C>T | ||
| ENST00000640681.1:n.553C>T | ||
| ENST00000652046.1:c.432C>T MANE Select | ENSP00000498466.1:p.Asp144= | |
| ENST00000313771.9:n.741C>T | ||
| ENST00000352159.8:c.432C>T | ENSP00000345601.4:p.Asp144= | |
| ENST00000355279.2:c.432C>T | ENSP00000347426.2:p.Asp144= | |
| ENST00000355740.6:c.432C>T | ENSP00000347979.2:p.Asp144= | |
| ENST00000357339.6:c.432C>T | ENSP00000349896.2:p.Asp144= | |
| ENST00000371857.7:n.598C>T | ||
| ENST00000460510.5:n.799C>T | ||
| ENST00000466081.5:n.503+1149C>T | ||
| ENST00000477270.5:n.595C>T | ||
| ENST00000479522.5:c.197-1553C>T | ENSP00000424113.1:n.197-1553C>T | |
| ENST00000484444.5:c.197-1553C>T | ENSP00000420975.1:n.197-1553C>T | |
| ENST00000487314.1:n.581C>T | ||
| ENST00000488877.5:c.334+1149C>T | ENSP00000425159.1:n.334+1149C>T | |
| ENST00000492756.5:c.334+1149C>T | ENSP00000422453.1:n.334+1149C>T | |
| ENST00000494410.5:c.334+1149C>T | ENSP00000423755.1:n.334+1149C>T | |
| ENST00000494799.5:n.351-1553C>T | ||
| ENST00000612663.4:c.432C>T | ENSP00000477997.2:p.Asp144= | |
| ENST00000615406.4:c.432C>T | ENSP00000484575.1:p.Asp144= | |
| ENST00000626542.2:c.432C>T | ENSP00000485876.1:p.Asp144= | |
| NM_000043.4:c.432C>T , LRG_134t1:c.432C>T | NP_000034.1:p.Asp144= | |
| NM_152871.2:c.432C>T | NP_690610.1:p.Asp144= | |
| NM_152872.2:c.432C>T | NP_690611.1:p.Asp144= | |
| NR_028033.2:n.680+1149C>T | ||
| NR_028034.2:n.543-1553C>T | ||
| NR_028035.2:n.543-1553C>T | ||
| NR_028036.2:n.680+1149C>T | ||
| XM_006717819.2:c.513C>T | XP_006717882.1:p.Asp171= | |
| XM_011539764.1:c.594C>T | XP_011538066.1:p.Asp198= | |
| XM_011539765.1:c.594C>T | XP_011538067.1:p.Asp198= | |
| XM_011539766.1:c.513C>T | XP_011538068.1:p.Asp171= | |
| XM_011539767.1:c.477C>T | XP_011538069.1:p.Asp159= | |
| XR_945732.1:n.511+1149C>T | ||
| XR_945733.1:n.511+1149C>T | ||
| NM_000043.5:c.432C>T | NP_000034.1:p.Asp144= | |
| NM_001320619.1:c.432C>T | NP_001307548.1:p.Asp144= | |
| NM_152871.3:c.432C>T | NP_690610.1:p.Asp144= | |
| NM_152872.3:c.432C>T | NP_690611.1:p.Asp144= | |
| NR_028033.3:n.652+1149C>T | ||
| NR_028034.3:n.515-1553C>T | ||
| NR_028035.3:n.515-1553C>T | ||
| NR_028036.3:n.652+1149C>T | ||
| NR_135313.1:n.652+1149C>T | ||
| NR_135314.1:n.741C>T | ||
| NR_135315.1:n.506-1553C>T | ||
| XM_006717819.3:c.513C>T | XP_006717882.1:p.Asp171= | |
| XM_011539764.2:c.594C>T | XP_011538066.1:p.Asp198= | |
| XM_011539765.2:c.594C>T | XP_011538067.1:p.Asp198= | |
| XM_011539766.2:c.513C>T | XP_011538068.1:p.Asp171= | |
| XM_011539767.3:c.477C>T | XP_011538069.1:p.Asp159= | |
| XR_945732.3:n.511+1149C>T | ||
| XR_945733.2:n.511+1149C>T | ||
| NM_000043.6:c.432C>T MANE Select | NP_000034.1:p.Asp144= | |
| NM_001320619.2:c.432C>T | NP_001307548.1:p.Asp144= | |
| NM_152871.4:c.432C>T | NP_690610.1:p.Asp144= | |
| NM_152872.4:c.432C>T | NP_690611.1:p.Asp144= | |
| NR_028033.4:n.413+1149C>T | ||
| NR_028034.4:n.276-1553C>T | ||
| NR_028035.4:n.276-1553C>T | ||
| NR_028036.4:n.413+1149C>T | ||
| NR_135313.2:n.413+1149C>T | ||
| NR_135314.2:n.598C>T | ||
| NR_135315.2:n.363-1553C>T |