MyVariant.info:
GRCh37
chr10:g.96058311C>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94298554C>G , CM000672.2:g.94298554C>G | GRCh38 |
| NC_000010.10:g.96058311C>G , CM000672.1:g.96058311C>G | GRCh37 |
| NC_000010.9:g.96048301C>G | NCBI36 |
| NG_015799.1:g.309566C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.4419C>G | ENSP00000360426.1:p.Ala1473= | |
| ENST00000685253.1:c.*1886C>G | ENSP00000509405.1:n.*1886C>G | |
| ENST00000685889.1:n.2078C>G | ||
| ENST00000686807.1:n.762C>G | ||
| ENST00000686954.1:c.*627C>G | ENSP00000508416.1:n.*627C>G | |
| ENST00000688810.1:c.4371C>G | ENSP00000509140.1:p.Ala1457= | |
| ENST00000689233.1:n.9551C>G | ||
| ENST00000690340.1:n.3016C>G | ||
| ENST00000692286.1:c.5211C>G | ENSP00000509490.1:p.Ala1737= | |
| ENST00000692396.1:c.5295C>G | ENSP00000508605.1:p.Ala1765= | |
| ENST00000371380.8:c.5343C>G MANE Select | ENSP00000360431.2:p.Ala1781= | |
| ENST00000371385.8:c.4317C>G | ENSP00000360438.4:p.Ala1439= | |
| ENST00000674738.1:c.3898C>G | ||
| ENST00000674827.1:c.3459C>G | ENSP00000502523.1:p.Ala1153= | |
| ENST00000675218.1:c.4419C>G | ENSP00000501910.1:p.Ala1473= | |
| ENST00000675487.1:c.*1276C>G | ENSP00000502340.1:n.*1276C>G | |
| ENST00000675718.1:c.4612C>G | ||
| ENST00000260766.7:c.5343C>G | ENSP00000260766.3:p.Ala1781= | |
| ENST00000371375.1:c.4419C>G | ENSP00000360426.1:p.Ala1473= | |
| ENST00000371380.7:c.5343C>G | ENSP00000360431.2:p.Ala1781= | |
| ENST00000371385.7:c.4419C>G | ENSP00000360438.3:p.Ala1473= | |
| NM_001165979.2:c.4419C>G | NP_001159451.1:p.Ala1473= | |
| NM_001288989.1:c.5295C>G | NP_001275918.1:p.Ala1765= | |
| NM_016341.3:c.5343C>G | NP_057425.3:p.Ala1781= | |
| XM_006717885.2:c.5385C>G | XP_006717948.1:p.Ala1795= | |
| XM_006717886.2:c.5385C>G | XP_006717949.1:p.Ala1795= | |
| XM_006717888.2:c.5382C>G | XP_006717951.1:p.Ala1794= | |
| XM_006717889.2:c.5337C>G | XP_006717952.1:p.Ala1779= | |
| XM_006717890.1:c.4461C>G | XP_006717953.1:p.Ala1487= | |
| XM_011539849.1:c.5385C>G | XP_011538151.1:p.Ala1795= | |
| XM_011539850.1:c.4230C>G | XP_011538152.1:p.Ala1410= | |
| XM_006717885.4:c.5385C>G | XP_006717948.1:p.Ala1795= | |
| XM_006717888.4:c.5382C>G | XP_006717951.1:p.Ala1794= | |
| XM_006717889.4:c.5337C>G | XP_006717952.1:p.Ala1779= | |
| XM_006717890.3:c.4461C>G | XP_006717953.1:p.Ala1487= | |
| XM_011539849.3:c.5385C>G | XP_011538151.1:p.Ala1795= | |
| XM_011539850.3:c.4230C>G | XP_011538152.1:p.Ala1410= | |
| XM_017016310.2:c.5385C>G | XP_016871799.1:p.Ala1795= | |
| XM_017016311.2:c.5385C>G | XP_016871800.1:p.Ala1795= | |
| XM_017016312.2:c.4371C>G | XP_016871801.1:p.Ala1457= | |
| NM_001288989.2:c.5295C>G | NP_001275918.1:p.Ala1765= | |
| NM_016341.4:c.5343C>G MANE Select | NP_057425.3:p.Ala1781= |