Linked Data
ClinVar Variation Id:
411385
dbSNP Id:
rs141298709
ExAC:
5:112176438 A / G
gnomAD v2:
5-112176438-A-G
gnomAD v3:
5-112840741-A-G
gnomAD v4:
5-112840741-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840741A>G , CM000667.2:g.112840741A>G | GRCh38 |
| NC_000005.9:g.112176438A>G , CM000667.1:g.112176438A>G | GRCh37 |
| NC_000005.8:g.112204337A>G | NCBI36 |
| NG_008481.4:g.153221A>G , LRG_130:g.153221A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5201A>G | ENSP00000473355.2:p.Asn1734Ser | |
| ENST00000505350.2:c.*5153A>G | ENSP00000481752.1:n.*5153A>G | |
| ENST00000507379.6:c.5093A>G | ENSP00000423224.2:p.Asn1698Ser | |
| ENST00000509732.6:c.5147A>G | ENSP00000426541.2:p.Asn1716Ser | |
| ENST00000512211.7:c.5147A>G | ENSP00000423828.3:p.Asn1716Ser | |
| ENST00000257430.9:c.5147A>G MANE Select | ENSP00000257430.4:p.Asn1716Ser | |
| ENST00000257430.8:c.5147A>G | ENSP00000257430.4:p.Asn1716Ser | |
| ENST00000508376.6:c.5147A>G | ENSP00000427089.2:p.Asn1716Ser | |
| ENST00000508624.5:c.*4469A>G | ENSP00000424265.1:n.*4469A>G | |
| ENST00000520401.1:c.230+11769A>G | ||
| NM_000038.5:c.5147A>G | NP_000029.2:p.Asn1716Ser | |
| NM_001127510.2:c.5147A>G | NP_001120982.1:p.Asn1716Ser | |
| NM_001127511.2:c.5093A>G | NP_001120983.2:p.Asn1698Ser | |
| NM_001354895.1:c.5147A>G | NP_001341824.1:p.Asn1716Ser | |
| NM_001354896.1:c.5201A>G | NP_001341825.1:p.Asn1734Ser | |
| NM_001354897.1:c.5177A>G | NP_001341826.1:p.Asn1726Ser | |
| NM_001354898.1:c.5072A>G | NP_001341827.1:p.Asn1691Ser | |
| NM_001354899.1:c.5063A>G | NP_001341828.1:p.Asn1688Ser | |
| NM_001354900.1:c.5024A>G | NP_001341829.1:p.Asn1675Ser | |
| NM_001354901.1:c.4970A>G | NP_001341830.1:p.Asn1657Ser | |
| NM_001354902.1:c.4874A>G | NP_001341831.1:p.Asn1625Ser | |
| NM_001354903.1:c.4844A>G | NP_001341832.1:p.Asn1615Ser | |
| NM_001354904.1:c.4769A>G | NP_001341833.1:p.Asn1590Ser | |
| NM_001354905.1:c.4667A>G | NP_001341834.1:p.Asn1556Ser | |
| NM_001354906.1:c.4298A>G | NP_001341835.1:p.Asn1433Ser | |
| NM_000038.6:c.5147A>G MANE Select | NP_000029.2:p.Asn1716Ser | |
| NM_001127510.3:c.5147A>G | NP_001120982.1:p.Asn1716Ser | |
| NM_001127511.3:c.5093A>G | NP_001120983.2:p.Asn1698Ser | |
| NM_001354895.2:c.5147A>G | NP_001341824.1:p.Asn1716Ser | |
| NM_001354896.2:c.5201A>G | NP_001341825.1:p.Asn1734Ser | |
| NM_001354897.2:c.5177A>G | NP_001341826.1:p.Asn1726Ser | |
| NM_001354898.2:c.5072A>G | NP_001341827.1:p.Asn1691Ser | |
| NM_001354899.2:c.5063A>G | NP_001341828.1:p.Asn1688Ser | |
| NM_001354900.2:c.5024A>G | NP_001341829.1:p.Asn1675Ser | |
| NM_001354901.2:c.4970A>G | NP_001341830.1:p.Asn1657Ser | |
| NM_001354902.2:c.4874A>G | NP_001341831.1:p.Asn1625Ser | |
| NM_001354903.2:c.4844A>G | NP_001341832.1:p.Asn1615Ser | |
| NM_001354904.2:c.4769A>G | NP_001341833.1:p.Asn1590Ser | |
| NM_001354905.2:c.4667A>G | NP_001341834.1:p.Asn1556Ser | |
| NM_001354906.2:c.4298A>G | NP_001341835.1:p.Asn1433Ser |