MyVariant.info:
GRCh37
chr10:g.96058299C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94298542C>A , CM000672.2:g.94298542C>A | GRCh38 |
| NC_000010.10:g.96058299C>A , CM000672.1:g.96058299C>A | GRCh37 |
| NC_000010.9:g.96048289C>A | NCBI36 |
| NG_015799.1:g.309554C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.4407C>A | ENSP00000360426.1:p.Thr1469= | |
| ENST00000685253.1:c.*1874C>A | ENSP00000509405.1:n.*1874C>A | |
| ENST00000685889.1:n.2066C>A | ||
| ENST00000686807.1:n.750C>A | ||
| ENST00000686954.1:c.*615C>A | ENSP00000508416.1:n.*615C>A | |
| ENST00000688810.1:c.4359C>A | ENSP00000509140.1:p.Thr1453= | |
| ENST00000689233.1:n.9539C>A | ||
| ENST00000690340.1:n.3004C>A | ||
| ENST00000692286.1:c.5199C>A | ENSP00000509490.1:p.Thr1733= | |
| ENST00000692396.1:c.5283C>A | ENSP00000508605.1:p.Thr1761= | |
| ENST00000371380.8:c.5331C>A MANE Select | ENSP00000360431.2:p.Thr1777= | |
| ENST00000371385.8:c.4305C>A | ENSP00000360438.4:p.Thr1435= | |
| ENST00000674738.1:c.3886C>A | ||
| ENST00000674827.1:c.3447C>A | ENSP00000502523.1:p.Thr1149= | |
| ENST00000675218.1:c.4407C>A | ENSP00000501910.1:p.Thr1469= | |
| ENST00000675487.1:c.*1264C>A | ENSP00000502340.1:n.*1264C>A | |
| ENST00000675718.1:c.4600C>A | ||
| ENST00000260766.7:c.5331C>A | ENSP00000260766.3:p.Thr1777= | |
| ENST00000371375.1:c.4407C>A | ENSP00000360426.1:p.Thr1469= | |
| ENST00000371380.7:c.5331C>A | ENSP00000360431.2:p.Thr1777= | |
| ENST00000371385.7:c.4407C>A | ENSP00000360438.3:p.Thr1469= | |
| NM_001165979.2:c.4407C>A | NP_001159451.1:p.Thr1469= | |
| NM_001288989.1:c.5283C>A | NP_001275918.1:p.Thr1761= | |
| NM_016341.3:c.5331C>A | NP_057425.3:p.Thr1777= | |
| XM_006717885.2:c.5373C>A | XP_006717948.1:p.Thr1791= | |
| XM_006717886.2:c.5373C>A | XP_006717949.1:p.Thr1791= | |
| XM_006717888.2:c.5370C>A | XP_006717951.1:p.Thr1790= | |
| XM_006717889.2:c.5325C>A | XP_006717952.1:p.Thr1775= | |
| XM_006717890.1:c.4449C>A | XP_006717953.1:p.Thr1483= | |
| XM_011539849.1:c.5373C>A | XP_011538151.1:p.Thr1791= | |
| XM_011539850.1:c.4218C>A | XP_011538152.1:p.Thr1406= | |
| XM_006717885.4:c.5373C>A | XP_006717948.1:p.Thr1791= | |
| XM_006717888.4:c.5370C>A | XP_006717951.1:p.Thr1790= | |
| XM_006717889.4:c.5325C>A | XP_006717952.1:p.Thr1775= | |
| XM_006717890.3:c.4449C>A | XP_006717953.1:p.Thr1483= | |
| XM_011539849.3:c.5373C>A | XP_011538151.1:p.Thr1791= | |
| XM_011539850.3:c.4218C>A | XP_011538152.1:p.Thr1406= | |
| XM_017016310.2:c.5373C>A | XP_016871799.1:p.Thr1791= | |
| XM_017016311.2:c.5373C>A | XP_016871800.1:p.Thr1791= | |
| XM_017016312.2:c.4359C>A | XP_016871801.1:p.Thr1453= | |
| NM_001288989.2:c.5283C>A | NP_001275918.1:p.Thr1761= | |
| NM_016341.4:c.5331C>A MANE Select | NP_057425.3:p.Thr1777= |