Linked Data
ClinVar Variation Id:
377493
dbSNP Id:
rs964029262
gnomAD v4:
5-112840007-A-G
COSMIC:
COSM4653877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840007A>G , CM000667.2:g.112840007A>G | GRCh38 |
| NC_000005.9:g.112175704A>G , CM000667.1:g.112175704A>G | GRCh37 |
| NC_000005.8:g.112203603A>G | NCBI36 |
| NG_008481.4:g.152487A>G , LRG_130:g.152487A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.4467A>G | ENSP00000473355.2:p.Ala1489= | |
| ENST00000505350.2:c.*4419A>G | ENSP00000481752.1:n.*4419A>G | |
| ENST00000507379.6:c.4359A>G | ENSP00000423224.2:p.Ala1453= | |
| ENST00000509732.6:c.4413A>G | ENSP00000426541.2:p.Ala1471= | |
| ENST00000512211.7:c.4413A>G | ENSP00000423828.3:p.Ala1471= | |
| ENST00000257430.9:c.4413A>G MANE Select | ENSP00000257430.4:p.Ala1471= | |
| ENST00000257430.8:c.4413A>G | ENSP00000257430.4:p.Ala1471= | |
| ENST00000508376.6:c.4413A>G | ENSP00000427089.2:p.Ala1471= | |
| ENST00000508624.5:c.*3735A>G | ENSP00000424265.1:n.*3735A>G | |
| ENST00000520401.1:c.230+11035A>G | ||
| NM_000038.5:c.4413A>G | NP_000029.2:p.Ala1471= | |
| NM_001127510.2:c.4413A>G | NP_001120982.1:p.Ala1471= | |
| NM_001127511.2:c.4359A>G | NP_001120983.2:p.Ala1453= | |
| NM_001354895.1:c.4413A>G | NP_001341824.1:p.Ala1471= | |
| NM_001354896.1:c.4467A>G | NP_001341825.1:p.Ala1489= | |
| NM_001354897.1:c.4443A>G | NP_001341826.1:p.Ala1481= | |
| NM_001354898.1:c.4338A>G | NP_001341827.1:p.Ala1446= | |
| NM_001354899.1:c.4329A>G | NP_001341828.1:p.Ala1443= | |
| NM_001354900.1:c.4290A>G | NP_001341829.1:p.Ala1430= | |
| NM_001354901.1:c.4236A>G | NP_001341830.1:p.Ala1412= | |
| NM_001354902.1:c.4140A>G | NP_001341831.1:p.Ala1380= | |
| NM_001354903.1:c.4110A>G | NP_001341832.1:p.Ala1370= | |
| NM_001354904.1:c.4035A>G | NP_001341833.1:p.Ala1345= | |
| NM_001354905.1:c.3933A>G | NP_001341834.1:p.Ala1311= | |
| NM_001354906.1:c.3564A>G | NP_001341835.1:p.Ala1188= | |
| NM_000038.6:c.4413A>G MANE Select | NP_000029.2:p.Ala1471= | |
| NM_001127510.3:c.4413A>G | NP_001120982.1:p.Ala1471= | |
| NM_001127511.3:c.4359A>G | NP_001120983.2:p.Ala1453= | |
| NM_001354895.2:c.4413A>G | NP_001341824.1:p.Ala1471= | |
| NM_001354896.2:c.4467A>G | NP_001341825.1:p.Ala1489= | |
| NM_001354897.2:c.4443A>G | NP_001341826.1:p.Ala1481= | |
| NM_001354898.2:c.4338A>G | NP_001341827.1:p.Ala1446= | |
| NM_001354899.2:c.4329A>G | NP_001341828.1:p.Ala1443= | |
| NM_001354900.2:c.4290A>G | NP_001341829.1:p.Ala1430= | |
| NM_001354901.2:c.4236A>G | NP_001341830.1:p.Ala1412= | |
| NM_001354902.2:c.4140A>G | NP_001341831.1:p.Ala1380= | |
| NM_001354903.2:c.4110A>G | NP_001341832.1:p.Ala1370= | |
| NM_001354904.2:c.4035A>G | NP_001341833.1:p.Ala1345= | |
| NM_001354905.2:c.3933A>G | NP_001341834.1:p.Ala1311= | |
| NM_001354906.2:c.3564A>G | NP_001341835.1:p.Ala1188= |