MyVariant.info:
GRCh37
chr10:g.96058314T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94298557T>C , CM000672.2:g.94298557T>C | GRCh38 |
| NC_000010.10:g.96058314T>C , CM000672.1:g.96058314T>C | GRCh37 |
| NC_000010.9:g.96048304T>C | NCBI36 |
| NG_015799.1:g.309569T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.4422T>C | ENSP00000360426.1:p.Cys1474= | |
| ENST00000685253.1:c.*1889T>C | ENSP00000509405.1:n.*1889T>C | |
| ENST00000685889.1:n.2081T>C | ||
| ENST00000686807.1:n.765T>C | ||
| ENST00000686954.1:c.*630T>C | ENSP00000508416.1:n.*630T>C | |
| ENST00000688810.1:c.4374T>C | ENSP00000509140.1:p.Cys1458= | |
| ENST00000689233.1:n.9554T>C | ||
| ENST00000690340.1:n.3019T>C | ||
| ENST00000692286.1:c.5214T>C | ENSP00000509490.1:p.Cys1738= | |
| ENST00000692396.1:c.5298T>C | ENSP00000508605.1:p.Cys1766= | |
| ENST00000371380.8:c.5346T>C MANE Select | ENSP00000360431.2:p.Cys1782= | |
| ENST00000371385.8:c.4320T>C | ENSP00000360438.4:p.Cys1440= | |
| ENST00000674738.1:c.3901T>C | ||
| ENST00000674827.1:c.3462T>C | ENSP00000502523.1:p.Cys1154= | |
| ENST00000675218.1:c.4422T>C | ENSP00000501910.1:p.Cys1474= | |
| ENST00000675487.1:c.*1279T>C | ENSP00000502340.1:n.*1279T>C | |
| ENST00000675718.1:c.4615T>C | ||
| ENST00000260766.7:c.5346T>C | ENSP00000260766.3:p.Cys1782= | |
| ENST00000371375.1:c.4422T>C | ENSP00000360426.1:p.Cys1474= | |
| ENST00000371380.7:c.5346T>C | ENSP00000360431.2:p.Cys1782= | |
| ENST00000371385.7:c.4422T>C | ENSP00000360438.3:p.Cys1474= | |
| NM_001165979.2:c.4422T>C | NP_001159451.1:p.Cys1474= | |
| NM_001288989.1:c.5298T>C | NP_001275918.1:p.Cys1766= | |
| NM_016341.3:c.5346T>C | NP_057425.3:p.Cys1782= | |
| XM_006717885.2:c.5388T>C | XP_006717948.1:p.Cys1796= | |
| XM_006717886.2:c.5388T>C | XP_006717949.1:p.Cys1796= | |
| XM_006717888.2:c.5385T>C | XP_006717951.1:p.Cys1795= | |
| XM_006717889.2:c.5340T>C | XP_006717952.1:p.Cys1780= | |
| XM_006717890.1:c.4464T>C | XP_006717953.1:p.Cys1488= | |
| XM_011539849.1:c.5388T>C | XP_011538151.1:p.Cys1796= | |
| XM_011539850.1:c.4233T>C | XP_011538152.1:p.Cys1411= | |
| XM_006717885.4:c.5388T>C | XP_006717948.1:p.Cys1796= | |
| XM_006717888.4:c.5385T>C | XP_006717951.1:p.Cys1795= | |
| XM_006717889.4:c.5340T>C | XP_006717952.1:p.Cys1780= | |
| XM_006717890.3:c.4464T>C | XP_006717953.1:p.Cys1488= | |
| XM_011539849.3:c.5388T>C | XP_011538151.1:p.Cys1796= | |
| XM_011539850.3:c.4233T>C | XP_011538152.1:p.Cys1411= | |
| XM_017016310.2:c.5388T>C | XP_016871799.1:p.Cys1796= | |
| XM_017016311.2:c.5388T>C | XP_016871800.1:p.Cys1796= | |
| XM_017016312.2:c.4374T>C | XP_016871801.1:p.Cys1458= | |
| NM_001288989.2:c.5298T>C | NP_001275918.1:p.Cys1766= | |
| NM_016341.4:c.5346T>C MANE Select | NP_057425.3:p.Cys1782= |