Linked Data
ClinVar Variation Id:
1369536
ClinVar RCV Id:
RCV001870683
dbSNP Id:
rs2149922916
gnomAD v4:
5-112840347-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840347A>G , CM000667.2:g.112840347A>G | GRCh38 |
| NC_000005.9:g.112176044A>G , CM000667.1:g.112176044A>G | GRCh37 |
| NC_000005.8:g.112203943A>G | NCBI36 |
| NG_008481.4:g.152827A>G , LRG_130:g.152827A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.4807A>G | ENSP00000473355.2:p.Thr1603Ala | |
| ENST00000505350.2:c.*4759A>G | ENSP00000481752.1:n.*4759A>G | |
| ENST00000507379.6:c.4699A>G | ENSP00000423224.2:p.Thr1567Ala | |
| ENST00000509732.6:c.4753A>G | ENSP00000426541.2:p.Thr1585Ala | |
| ENST00000512211.7:c.4753A>G | ENSP00000423828.3:p.Thr1585Ala | |
| ENST00000257430.9:c.4753A>G MANE Select | ENSP00000257430.4:p.Thr1585Ala | |
| ENST00000257430.8:c.4753A>G | ENSP00000257430.4:p.Thr1585Ala | |
| ENST00000508376.6:c.4753A>G | ENSP00000427089.2:p.Thr1585Ala | |
| ENST00000508624.5:c.*4075A>G | ENSP00000424265.1:n.*4075A>G | |
| ENST00000520401.1:c.230+11375A>G | ||
| NM_000038.5:c.4753A>G | NP_000029.2:p.Thr1585Ala | |
| NM_001127510.2:c.4753A>G | NP_001120982.1:p.Thr1585Ala | |
| NM_001127511.2:c.4699A>G | NP_001120983.2:p.Thr1567Ala | |
| NM_001354895.1:c.4753A>G | NP_001341824.1:p.Thr1585Ala | |
| NM_001354896.1:c.4807A>G | NP_001341825.1:p.Thr1603Ala | |
| NM_001354897.1:c.4783A>G | NP_001341826.1:p.Thr1595Ala | |
| NM_001354898.1:c.4678A>G | NP_001341827.1:p.Thr1560Ala | |
| NM_001354899.1:c.4669A>G | NP_001341828.1:p.Thr1557Ala | |
| NM_001354900.1:c.4630A>G | NP_001341829.1:p.Thr1544Ala | |
| NM_001354901.1:c.4576A>G | NP_001341830.1:p.Thr1526Ala | |
| NM_001354902.1:c.4480A>G | NP_001341831.1:p.Thr1494Ala | |
| NM_001354903.1:c.4450A>G | NP_001341832.1:p.Thr1484Ala | |
| NM_001354904.1:c.4375A>G | NP_001341833.1:p.Thr1459Ala | |
| NM_001354905.1:c.4273A>G | NP_001341834.1:p.Thr1425Ala | |
| NM_001354906.1:c.3904A>G | NP_001341835.1:p.Thr1302Ala | |
| NM_000038.6:c.4753A>G MANE Select | NP_000029.2:p.Thr1585Ala | |
| NM_001127510.3:c.4753A>G | NP_001120982.1:p.Thr1585Ala | |
| NM_001127511.3:c.4699A>G | NP_001120983.2:p.Thr1567Ala | |
| NM_001354895.2:c.4753A>G | NP_001341824.1:p.Thr1585Ala | |
| NM_001354896.2:c.4807A>G | NP_001341825.1:p.Thr1603Ala | |
| NM_001354897.2:c.4783A>G | NP_001341826.1:p.Thr1595Ala | |
| NM_001354898.2:c.4678A>G | NP_001341827.1:p.Thr1560Ala | |
| NM_001354899.2:c.4669A>G | NP_001341828.1:p.Thr1557Ala | |
| NM_001354900.2:c.4630A>G | NP_001341829.1:p.Thr1544Ala | |
| NM_001354901.2:c.4576A>G | NP_001341830.1:p.Thr1526Ala | |
| NM_001354902.2:c.4480A>G | NP_001341831.1:p.Thr1494Ala | |
| NM_001354903.2:c.4450A>G | NP_001341832.1:p.Thr1484Ala | |
| NM_001354904.2:c.4375A>G | NP_001341833.1:p.Thr1459Ala | |
| NM_001354905.2:c.4273A>G | NP_001341834.1:p.Thr1425Ala | |
| NM_001354906.2:c.3904A>G | NP_001341835.1:p.Thr1302Ala |