Linked Data
ClinVar Variation Id:
1042148
dbSNP Id:
rs778283715
ExAC:
5:112176473 A / G
gnomAD v2:
5-112176473-A-G
gnomAD v4:
5-112840776-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840776A>G , CM000667.2:g.112840776A>G | GRCh38 |
| NC_000005.9:g.112176473A>G , CM000667.1:g.112176473A>G | GRCh37 |
| NC_000005.8:g.112204372A>G | NCBI36 |
| NG_008481.4:g.153256A>G , LRG_130:g.153256A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5236A>G | ENSP00000473355.2:p.Ile1746Val | |
| ENST00000505350.2:c.*5188A>G | ENSP00000481752.1:n.*5188A>G | |
| ENST00000507379.6:c.5128A>G | ENSP00000423224.2:p.Ile1710Val | |
| ENST00000509732.6:c.5182A>G | ENSP00000426541.2:p.Ile1728Val | |
| ENST00000512211.7:c.5182A>G | ENSP00000423828.3:p.Ile1728Val | |
| ENST00000257430.9:c.5182A>G MANE Select | ENSP00000257430.4:p.Ile1728Val | |
| ENST00000257430.8:c.5182A>G | ENSP00000257430.4:p.Ile1728Val | |
| ENST00000508376.6:c.5182A>G | ENSP00000427089.2:p.Ile1728Val | |
| ENST00000508624.5:c.*4504A>G | ENSP00000424265.1:n.*4504A>G | |
| ENST00000520401.1:c.230+11804A>G | ||
| NM_000038.5:c.5182A>G | NP_000029.2:p.Ile1728Val | |
| NM_001127510.2:c.5182A>G | NP_001120982.1:p.Ile1728Val | |
| NM_001127511.2:c.5128A>G | NP_001120983.2:p.Ile1710Val | |
| NM_001354895.1:c.5182A>G | NP_001341824.1:p.Ile1728Val | |
| NM_001354896.1:c.5236A>G | NP_001341825.1:p.Ile1746Val | |
| NM_001354897.1:c.5212A>G | NP_001341826.1:p.Ile1738Val | |
| NM_001354898.1:c.5107A>G | NP_001341827.1:p.Ile1703Val | |
| NM_001354899.1:c.5098A>G | NP_001341828.1:p.Ile1700Val | |
| NM_001354900.1:c.5059A>G | NP_001341829.1:p.Ile1687Val | |
| NM_001354901.1:c.5005A>G | NP_001341830.1:p.Ile1669Val | |
| NM_001354902.1:c.4909A>G | NP_001341831.1:p.Ile1637Val | |
| NM_001354903.1:c.4879A>G | NP_001341832.1:p.Ile1627Val | |
| NM_001354904.1:c.4804A>G | NP_001341833.1:p.Ile1602Val | |
| NM_001354905.1:c.4702A>G | NP_001341834.1:p.Ile1568Val | |
| NM_001354906.1:c.4333A>G | NP_001341835.1:p.Ile1445Val | |
| NM_000038.6:c.5182A>G MANE Select | NP_000029.2:p.Ile1728Val | |
| NM_001127510.3:c.5182A>G | NP_001120982.1:p.Ile1728Val | |
| NM_001127511.3:c.5128A>G | NP_001120983.2:p.Ile1710Val | |
| NM_001354895.2:c.5182A>G | NP_001341824.1:p.Ile1728Val | |
| NM_001354896.2:c.5236A>G | NP_001341825.1:p.Ile1746Val | |
| NM_001354897.2:c.5212A>G | NP_001341826.1:p.Ile1738Val | |
| NM_001354898.2:c.5107A>G | NP_001341827.1:p.Ile1703Val | |
| NM_001354899.2:c.5098A>G | NP_001341828.1:p.Ile1700Val | |
| NM_001354900.2:c.5059A>G | NP_001341829.1:p.Ile1687Val | |
| NM_001354901.2:c.5005A>G | NP_001341830.1:p.Ile1669Val | |
| NM_001354902.2:c.4909A>G | NP_001341831.1:p.Ile1637Val | |
| NM_001354903.2:c.4879A>G | NP_001341832.1:p.Ile1627Val | |
| NM_001354904.2:c.4804A>G | NP_001341833.1:p.Ile1602Val | |
| NM_001354905.2:c.4702A>G | NP_001341834.1:p.Ile1568Val | |
| NM_001354906.2:c.4333A>G | NP_001341835.1:p.Ile1445Val |