Linked Data
ClinVar Variation Id:
54291
dbSNP Id:
rs80357122
ExAC:
17:41245987 C / T
gnomAD v2:
17-41245987-C-T
gnomAD v3:
17-43093970-C-T
gnomAD v4:
17-43093970-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43093970C>T , CM000679.2:g.43093970C>T | GRCh38 |
| NC_000017.10:g.41245987C>T , CM000679.1:g.41245987C>T | GRCh37 |
| NC_000017.9:g.38499513C>T | NCBI36 |
| NG_005905.2:g.124014G>A , LRG_292:g.124014G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.1625G>A | ||
| ENST00000461574.2:c.1561G>A | ENSP00000417241.2:p.Ala521Thr | |
| ENST00000470026.6:c.1561G>A | ENSP00000419274.2:p.Ala521Thr | |
| ENST00000473961.6:c.1435G>A | ENSP00000420201.2:p.Ala479Thr | |
| ENST00000476777.6:c.1558G>A | ENSP00000417554.2:p.Ala520Thr | |
| ENST00000477152.6:c.1483G>A | ENSP00000419988.2:p.Ala495Thr | |
| ENST00000478531.6:c.784+774G>A | ENSP00000420412.2:n.784+774G>A | |
| ENST00000489037.2:c.1483G>A | ENSP00000420781.2:p.Ala495Thr | |
| ENST00000493919.6:c.646+774G>A | ENSP00000418819.2:n.646+774G>A | |
| ENST00000494123.6:c.1561G>A | ENSP00000419103.2:p.Ala521Thr | |
| ENST00000497488.2:c.673G>A | ENSP00000418986.2:p.Ala225Thr | |
| ENST00000618469.2:c.1561G>A | ENSP00000478114.2:p.Ala521Thr | |
| ENST00000634433.2:c.1438G>A | ENSP00000489431.2:p.Ala480Thr | |
| ENST00000644379.2:c.1561G>A | ENSP00000496570.2:p.Ala521Thr | |
| ENST00000644555.2:c.646+774G>A | ENSP00000494614.2:n.646+774G>A | |
| ENST00000652672.2:c.1420G>A | ENSP00000498906.2:p.Ala474Thr | |
| ENST00000484087.6:c.664+774G>A | ENSP00000419481.2:n.664+774G>A | |
| ENST00000700182.1:c.706+774G>A | ENSP00000514849.1:n.706+774G>A | |
| ENST00000357654.9:c.1561G>A MANE Select | ENSP00000350283.3:p.Ala521Thr | |
| ENST00000471181.7:c.1561G>A | ENSP00000418960.2:p.Ala521Thr | |
| ENST00000652672.1:c.1420G>A | ENSP00000498906.1:p.Ala474Thr | |
| ENST00000352993.7:c.670+1876G>A | ENSP00000312236.5:n.670+1876G>A | |
| ENST00000354071.7:c.1561G>A | ENSP00000326002.7:p.Ala521Thr | |
| ENST00000357654.7:c.1561G>A | ENSP00000350283.3:p.Ala521Thr | |
| ENST00000412061.3:c.912G>A | ||
| ENST00000461221.5:c.*1344G>A | ENSP00000418548.1:n.*1344G>A | |
| ENST00000468300.5:c.787+774G>A | ENSP00000417148.1:n.787+774G>A | |
| ENST00000470026.5:c.1561G>A | ENSP00000419274.1:p.Ala521Thr | |
| ENST00000471181.6:c.1561G>A | ENSP00000418960.2:p.Ala521Thr | |
| ENST00000477152.5:c.1483G>A | ENSP00000419988.1:p.Ala495Thr | |
| ENST00000478531.5:c.784+774G>A | ENSP00000420412.1:n.784+774G>A | |
| ENST00000484087.5:c.409+774G>A | ENSP00000419481.1:n.409+774G>A | |
| ENST00000487825.5:c.412+774G>A | ENSP00000418212.1:n.412+774G>A | |
| ENST00000491747.6:c.787+774G>A | ENSP00000420705.2:n.787+774G>A | |
| ENST00000493795.5:c.1420G>A | ENSP00000418775.1:p.Ala474Thr | |
| ENST00000493919.5:c.646+774G>A | ENSP00000418819.1:n.646+774G>A | |
| ENST00000586385.5:c.5-30019G>A | ENSP00000465818.1:n.5-30019G>A | |
| ENST00000591534.5:c.-43-19449G>A | ENSP00000467329.1:n.-43-19449G>A | |
| ENST00000591849.5:c.-99+31301G>A | ENSP00000465347.1:n.-99+31301G>A | |
| ENST00000634433.1:c.1438G>A | ENSP00000489431.1:p.Ala480Thr | |
| NM_007294.3:c.1561G>A , LRG_292t1:c.1561G>A | NP_009225.1:p.Ala521Thr | |
| NM_007297.3:c.1420G>A | NP_009228.2:p.Ala474Thr | |
| NM_007298.3:c.787+774G>A | NP_009229.2:n.787+774G>A | |
| NM_007299.3:c.787+774G>A | NP_009230.2:n.787+774G>A | |
| NM_007300.3:c.1561G>A | NP_009231.2:p.Ala521Thr | |
| NR_027676.1:n.1697G>A | ||
| NM_007294.4:c.1561G>A MANE Select | NP_009225.1:p.Ala521Thr | |
| NM_007297.4:c.1420G>A | NP_009228.2:p.Ala474Thr | |
| NM_007299.4:c.787+774G>A | NP_009230.2:n.787+774G>A | |
| NM_007300.4:c.1561G>A | NP_009231.2:p.Ala521Thr | |
| NR_027676.2:n.1738G>A |