MyVariant.info:
GRCh37
chr10:g.96058341C>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94298584C>A , CM000672.2:g.94298584C>A | GRCh38 |
| NC_000010.10:g.96058341C>A , CM000672.1:g.96058341C>A | GRCh37 |
| NC_000010.9:g.96048331C>A | NCBI36 |
| NG_015799.1:g.309596C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.4449C>A | ENSP00000360426.1:p.Ala1483= | |
| ENST00000685253.1:c.*1916C>A | ENSP00000509405.1:n.*1916C>A | |
| ENST00000685889.1:n.2108C>A | ||
| ENST00000686807.1:n.792C>A | ||
| ENST00000686954.1:c.*657C>A | ENSP00000508416.1:n.*657C>A | |
| ENST00000688810.1:c.4401C>A | ENSP00000509140.1:p.Ala1467= | |
| ENST00000689233.1:n.9581C>A | ||
| ENST00000690340.1:n.3046C>A | ||
| ENST00000692286.1:c.5241C>A | ENSP00000509490.1:p.Ala1747= | |
| ENST00000692396.1:c.5325C>A | ENSP00000508605.1:p.Ala1775= | |
| ENST00000371380.8:c.5373C>A MANE Select | ENSP00000360431.2:p.Ala1791= | |
| ENST00000371385.8:c.4347C>A | ENSP00000360438.4:p.Ala1449= | |
| ENST00000674738.1:c.3928C>A | ||
| ENST00000674827.1:c.3489C>A | ENSP00000502523.1:p.Ala1163= | |
| ENST00000675218.1:c.4449C>A | ENSP00000501910.1:p.Ala1483= | |
| ENST00000675487.1:c.*1306C>A | ENSP00000502340.1:n.*1306C>A | |
| ENST00000675718.1:c.4642C>A | ||
| ENST00000260766.7:c.5373C>A | ENSP00000260766.3:p.Ala1791= | |
| ENST00000371375.1:c.4449C>A | ENSP00000360426.1:p.Ala1483= | |
| ENST00000371380.7:c.5373C>A | ENSP00000360431.2:p.Ala1791= | |
| ENST00000371385.7:c.4449C>A | ENSP00000360438.3:p.Ala1483= | |
| NM_001165979.2:c.4449C>A | NP_001159451.1:p.Ala1483= | |
| NM_001288989.1:c.5325C>A | NP_001275918.1:p.Ala1775= | |
| NM_016341.3:c.5373C>A | NP_057425.3:p.Ala1791= | |
| XM_006717885.2:c.5415C>A | XP_006717948.1:p.Ala1805= | |
| XM_006717886.2:c.5415C>A | XP_006717949.1:p.Ala1805= | |
| XM_006717888.2:c.5412C>A | XP_006717951.1:p.Ala1804= | |
| XM_006717889.2:c.5367C>A | XP_006717952.1:p.Ala1789= | |
| XM_006717890.1:c.4491C>A | XP_006717953.1:p.Ala1497= | |
| XM_011539849.1:c.5415C>A | XP_011538151.1:p.Ala1805= | |
| XM_011539850.1:c.4260C>A | XP_011538152.1:p.Ala1420= | |
| XM_006717885.4:c.5415C>A | XP_006717948.1:p.Ala1805= | |
| XM_006717888.4:c.5412C>A | XP_006717951.1:p.Ala1804= | |
| XM_006717889.4:c.5367C>A | XP_006717952.1:p.Ala1789= | |
| XM_006717890.3:c.4491C>A | XP_006717953.1:p.Ala1497= | |
| XM_011539849.3:c.5415C>A | XP_011538151.1:p.Ala1805= | |
| XM_011539850.3:c.4260C>A | XP_011538152.1:p.Ala1420= | |
| XM_017016310.2:c.5415C>A | XP_016871799.1:p.Ala1805= | |
| XM_017016311.2:c.5415C>A | XP_016871800.1:p.Ala1805= | |
| XM_017016312.2:c.4401C>A | XP_016871801.1:p.Ala1467= | |
| NM_001288989.2:c.5325C>A | NP_001275918.1:p.Ala1775= | |
| NM_016341.4:c.5373C>A MANE Select | NP_057425.3:p.Ala1791= |