ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.165992167T>A , CM000664.2:g.165992167T>A | GRCh38 |
| NC_000002.11:g.166848677T>A , CM000664.1:g.166848677T>A | GRCh37 |
| NC_000002.10:g.166556923T>A | NCBI36 |
| NG_011906.1:g.86473A>T , LRG_8:g.86473A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689288.1:c.*3144A>T | ENSP00000509637.1:n.*3144A>T | |
| ENST00000303395.9:c.5108A>T | ENSP00000303540.4:p.Asp1703Val | |
| ENST00000635750.1:c.5075A>T | ENSP00000490799.1:p.Asp1692Val | |
| ENST00000635776.1:c.*1941A>T | ENSP00000490692.1:n.*1941A>T | |
| ENST00000636194.1:c.*2601A>T | ENSP00000490288.1:n.*2601A>T | |
| ENST00000637038.1:c.1970A>T | ||
| ENST00000637988.1:c.5075A>T | ENSP00000490780.1:p.Asp1692Val | |
| ENST00000640036.1:c.5075A>T | ENSP00000491573.1:p.Asp1692Val | |
| ENST00000641575.1:c.5072A>T | ENSP00000492917.1:p.Asp1691Val | |
| ENST00000641603.1:c.4826A>T | ENSP00000492945.1:p.Asp1609Val | |
| ENST00000641996.1:c.*4662A>T | ENSP00000493054.1:n.*4662A>T | |
| ENST00000671940.1:c.*3051A>T | ENSP00000500336.1:n.*3051A>T | |
| ENST00000673490.1:n.7581A>T | ||
| ENST00000674923.1:c.5108A>T MANE Select | ENSP00000501589.1:p.Asp1703Val | |
| ENST00000303395.8:c.5108A>T | ENSP00000303540.4:p.Asp1703Val | |
| ENST00000375405.7:c.5075A>T | ENSP00000364554.3:p.Asp1692Val | |
| ENST00000409050.1:c.5024A>T | ENSP00000386312.1:p.Asp1675Val | |
| ENST00000423058.6:c.5108A>T | ENSP00000407030.2:p.Asp1703Val | |
| NM_001165963.1:c.5108A>T | NP_001159435.1:p.Asp1703Val | |
| NM_001165964.1:c.5024A>T | NP_001159436.1:p.Asp1675Val | |
| NM_001202435.1:c.5108A>T | NP_001189364.1:p.Asp1703Val | |
| NM_006920.4:c.5075A>T , LRG_8t1:c.5075A>T | NP_008851.3:p.Asp1692Val | |
| NR_110598.1:n.176-23446T>A | ||
| XM_011511598.1:c.5108A>T | XP_011509900.1:p.Asp1703Val | |
| XM_011511599.1:c.5108A>T | XP_011509901.1:p.Asp1703Val | |
| XM_011511600.1:c.5108A>T | XP_011509902.1:p.Asp1703Val | |
| XM_011511601.1:c.5108A>T | XP_011509903.1:p.Asp1703Val | |
| XM_011511602.1:c.5108A>T | XP_011509904.1:p.Asp1703Val | |
| XM_011511603.1:c.5105A>T | XP_011509905.1:p.Asp1702Val | |
| XM_011511604.1:c.5075A>T | XP_011509906.1:p.Asp1692Val | |
| XM_011511605.1:c.5072A>T | XP_011509907.1:p.Asp1691Val | |
| XM_011511606.1:c.5024A>T | XP_011509908.1:p.Asp1675Val | |
| XM_011511607.1:c.4826A>T | XP_011509909.1:p.Asp1609Val | |
| NM_001165963.2:c.5108A>T | NP_001159435.1:p.Asp1703Val | |
| NM_001165964.2:c.5024A>T | NP_001159436.1:p.Asp1675Val | |
| NM_001202435.2:c.5108A>T | NP_001189364.1:p.Asp1703Val | |
| NM_001353948.1:c.5108A>T | NP_001340877.1:p.Asp1703Val | |
| NM_001353949.1:c.5075A>T | NP_001340878.1:p.Asp1692Val | |
| NM_001353950.1:c.5075A>T | NP_001340879.1:p.Asp1692Val | |
| NM_001353951.1:c.5075A>T | NP_001340880.1:p.Asp1692Val | |
| NM_001353952.1:c.5075A>T | NP_001340881.1:p.Asp1692Val | |
| NM_001353954.1:c.5072A>T | NP_001340883.1:p.Asp1691Val | |
| NM_001353955.1:c.5072A>T | NP_001340884.1:p.Asp1691Val | |
| NM_001353957.1:c.5024A>T | NP_001340886.1:p.Asp1675Val | |
| NM_001353958.1:c.5024A>T | NP_001340887.1:p.Asp1675Val | |
| NM_001353960.1:c.5021A>T | NP_001340889.1:p.Asp1674Val | |
| NM_001353961.1:c.2666A>T | NP_001340890.1:p.Asp889Val | |
| NM_006920.5:c.5075A>T | NP_008851.3:p.Asp1692Val | |
| NR_148667.1:n.5544A>T | ||
| XR_001738883.1:n.5558A>T | ||
| XR_001738884.1:n.5530A>T | ||
| NM_001165963.3:c.5108A>T | NP_001159435.1:p.Asp1703Val | |
| NM_001165964.3:c.5024A>T | NP_001159436.1:p.Asp1675Val | |
| NM_001202435.3:c.5108A>T | NP_001189364.1:p.Asp1703Val | |
| NM_001353948.2:c.5108A>T | NP_001340877.1:p.Asp1703Val | |
| NM_001353949.2:c.5075A>T | NP_001340878.1:p.Asp1692Val | |
| NM_001353950.2:c.5075A>T | NP_001340879.1:p.Asp1692Val | |
| NM_001353951.2:c.5075A>T | NP_001340880.1:p.Asp1692Val | |
| NM_001353952.2:c.5075A>T | NP_001340881.1:p.Asp1692Val | |
| NM_001353954.2:c.5072A>T | NP_001340883.1:p.Asp1691Val | |
| NM_001353955.2:c.5072A>T | NP_001340884.1:p.Asp1691Val | |
| NM_001353957.2:c.5024A>T | NP_001340886.1:p.Asp1675Val | |
| NM_001353958.2:c.5024A>T | NP_001340887.1:p.Asp1675Val | |
| NM_001353960.2:c.5021A>T | NP_001340889.1:p.Asp1674Val | |
| NM_001353961.2:c.2666A>T | NP_001340890.1:p.Asp889Val | |
| NM_006920.6:c.5075A>T | NP_008851.3:p.Asp1692Val | |
| NR_148667.2:n.5525A>T | ||
| NM_001165963.4:c.5108A>T MANE Select | NP_001159435.1:p.Asp1703Val |