Linked Data
ClinVar Variation Id:
537485
dbSNP Id:
rs587782868
ExAC:
5:112163648 G / A
gnomAD v2:
5-112163648-G-A
gnomAD v3:
5-112827951-G-A
gnomAD v4:
5-112827951-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112827951G>A , CM000667.2:g.112827951G>A | GRCh38 |
| NC_000005.9:g.112163648G>A , CM000667.1:g.112163648G>A | GRCh37 |
| NC_000005.8:g.112191547G>A | NCBI36 |
| NG_008481.4:g.140431G>A , LRG_130:g.140431G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1408+5960G>A | ENSP00000484935.2:n.1408+5960G>A | |
| ENST00000504915.3:c.1625G>A | ENSP00000473355.2:p.Gly542Asp | |
| ENST00000505084.2:n.1627G>A | ||
| ENST00000505350.2:c.*1577G>A | ENSP00000481752.1:n.*1577G>A | |
| ENST00000507379.6:c.1517G>A | ENSP00000423224.2:p.Gly506Asp | |
| ENST00000509732.6:c.1571G>A | ENSP00000426541.2:p.Gly524Asp | |
| ENST00000512211.7:c.1571G>A | ENSP00000423828.3:p.Gly524Asp | |
| ENST00000257430.9:c.1571G>A MANE Select | ENSP00000257430.4:p.Gly524Asp | |
| ENST00000257430.8:c.1571G>A | ENSP00000257430.4:p.Gly524Asp | |
| ENST00000502371.2:c.96+5960G>A | ||
| ENST00000504915.2:c.260G>A | ENSP00000473355.1:p.Gly87Asp | |
| ENST00000505084.1:n.58G>A | ||
| ENST00000507379.5:c.1517G>A | ENSP00000423224.1:p.Gly506Asp | |
| ENST00000508376.6:c.1571G>A | ENSP00000427089.2:p.Gly524Asp | |
| ENST00000508624.5:c.*893G>A | ENSP00000424265.1:n.*893G>A | |
| ENST00000512211.6:c.1571G>A | ENSP00000423828.2:p.Gly524Asp | |
| ENST00000520401.1:c.58G>A | ||
| NM_000038.5:c.1571G>A | NP_000029.2:p.Gly524Asp | |
| NM_001127510.2:c.1571G>A | NP_001120982.1:p.Gly524Asp | |
| NM_001127511.2:c.1517G>A | NP_001120983.2:p.Gly506Asp | |
| NM_001354895.1:c.1571G>A | NP_001341824.1:p.Gly524Asp | |
| NM_001354896.1:c.1625G>A | NP_001341825.1:p.Gly542Asp | |
| NM_001354897.1:c.1601G>A | NP_001341826.1:p.Gly534Asp | |
| NM_001354898.1:c.1496G>A | NP_001341827.1:p.Gly499Asp | |
| NM_001354899.1:c.1487G>A | NP_001341828.1:p.Gly496Asp | |
| NM_001354900.1:c.1448G>A | NP_001341829.1:p.Gly483Asp | |
| NM_001354901.1:c.1394G>A | NP_001341830.1:p.Gly465Asp | |
| NM_001354902.1:c.1298G>A | NP_001341831.1:p.Gly433Asp | |
| NM_001354903.1:c.1268G>A | NP_001341832.1:p.Gly423Asp | |
| NM_001354904.1:c.1193G>A | NP_001341833.1:p.Gly398Asp | |
| NM_001354905.1:c.1091G>A | NP_001341834.1:p.Gly364Asp | |
| NM_001354906.1:c.722G>A | NP_001341835.1:p.Gly241Asp | |
| NM_000038.6:c.1571G>A MANE Select | NP_000029.2:p.Gly524Asp | |
| NM_001127510.3:c.1571G>A | NP_001120982.1:p.Gly524Asp | |
| NM_001127511.3:c.1517G>A | NP_001120983.2:p.Gly506Asp | |
| NM_001354895.2:c.1571G>A | NP_001341824.1:p.Gly524Asp | |
| NM_001354896.2:c.1625G>A | NP_001341825.1:p.Gly542Asp | |
| NM_001354897.2:c.1601G>A | NP_001341826.1:p.Gly534Asp | |
| NM_001354898.2:c.1496G>A | NP_001341827.1:p.Gly499Asp | |
| NM_001354899.2:c.1487G>A | NP_001341828.1:p.Gly496Asp | |
| NM_001354900.2:c.1448G>A | NP_001341829.1:p.Gly483Asp | |
| NM_001354901.2:c.1394G>A | NP_001341830.1:p.Gly465Asp | |
| NM_001354902.2:c.1298G>A | NP_001341831.1:p.Gly433Asp | |
| NM_001354903.2:c.1268G>A | NP_001341832.1:p.Gly423Asp | |
| NM_001354904.2:c.1193G>A | NP_001341833.1:p.Gly398Asp | |
| NM_001354905.2:c.1091G>A | NP_001341834.1:p.Gly364Asp | |
| NM_001354906.2:c.722G>A | NP_001341835.1:p.Gly241Asp |