Linked Data
ClinVar Variation Id:
55641
dbSNP Id:
rs80357142
ExAC:
17:41249282 A / T
gnomAD v2:
17-41249282-A-T
gnomAD v4:
17-43097265-A-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43097265A>T , CM000679.2:g.43097265A>T | GRCh38 |
| NC_000017.10:g.41249282A>T , CM000679.1:g.41249282A>T | GRCh37 |
| NC_000017.9:g.38502808A>T | NCBI36 |
| NG_005905.2:g.120719T>A , LRG_292:g.120719T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354071.8:n.636T>A | ||
| ENST00000461574.2:c.572T>A | ENSP00000417241.2:p.Val191Asp | |
| ENST00000470026.6:c.572T>A | ENSP00000419274.2:p.Val191Asp | |
| ENST00000473961.6:c.545-2405T>A | ENSP00000420201.2:n.545-2405T>A | |
| ENST00000476777.6:c.569T>A | ENSP00000417554.2:p.Val190Asp | |
| ENST00000477152.6:c.494T>A | ENSP00000419988.2:p.Val165Asp | |
| ENST00000478531.6:c.569T>A | ENSP00000420412.2:p.Val190Asp | |
| ENST00000489037.2:c.494T>A | ENSP00000420781.2:p.Val165Asp | |
| ENST00000493919.6:c.431T>A | ENSP00000418819.2:p.Val144Asp | |
| ENST00000494123.6:c.572T>A | ENSP00000419103.2:p.Val191Asp | |
| ENST00000497488.2:c.-218-2405T>A | ENSP00000418986.2:n.-218-2405T>A | |
| ENST00000618469.2:c.572T>A | ENSP00000478114.2:p.Val191Asp | |
| ENST00000634433.2:c.548-2405T>A | ENSP00000489431.2:n.548-2405T>A | |
| ENST00000644379.2:c.572T>A | ENSP00000496570.2:p.Val191Asp | |
| ENST00000644555.2:c.431T>A | ENSP00000494614.2:p.Val144Asp | |
| ENST00000652672.2:c.431T>A | ENSP00000498906.2:p.Val144Asp | |
| ENST00000484087.6:c.548-2405T>A | ENSP00000419481.2:n.548-2405T>A | |
| ENST00000700182.1:c.491T>A | ENSP00000514849.1:p.Val164Asp | |
| ENST00000700183.1:c.*580T>A | ENSP00000514850.1:n.*580T>A | |
| ENST00000357654.9:c.572T>A MANE Select | ENSP00000350283.3:p.Val191Asp | |
| ENST00000471181.7:c.572T>A | ENSP00000418960.2:p.Val191Asp | |
| ENST00000642945.1:c.*446T>A | ENSP00000495897.1:n.*446T>A | |
| ENST00000652672.1:c.431T>A | ENSP00000498906.1:p.Val144Asp | |
| ENST00000352993.7:c.572T>A | ENSP00000312236.5:p.Val191Asp | |
| ENST00000354071.7:c.572T>A | ENSP00000326002.7:p.Val191Asp | |
| ENST00000357654.7:c.572T>A | ENSP00000350283.3:p.Val191Asp | |
| ENST00000461221.5:c.*355T>A | ENSP00000418548.1:n.*355T>A | |
| ENST00000468300.5:c.572T>A | ENSP00000417148.1:p.Val191Asp | |
| ENST00000470026.5:c.572T>A | ENSP00000419274.1:p.Val191Asp | |
| ENST00000471181.6:c.572T>A | ENSP00000418960.2:p.Val191Asp | |
| ENST00000473961.5:c.268-2405T>A | ||
| ENST00000476777.5:c.569T>A | ENSP00000417554.1:p.Val190Asp | |
| ENST00000477152.5:c.494T>A | ENSP00000419988.1:p.Val165Asp | |
| ENST00000478531.5:c.569T>A | ENSP00000420412.1:p.Val190Asp | |
| ENST00000484087.5:c.293-2405T>A | ENSP00000419481.1:n.293-2405T>A | |
| ENST00000487825.5:c.296-2405T>A | ENSP00000418212.1:n.296-2405T>A | |
| ENST00000491747.6:c.572T>A | ENSP00000420705.2:p.Val191Asp | |
| ENST00000492859.5:c.*508T>A | ENSP00000420253.1:n.*508T>A | |
| ENST00000493795.5:c.431T>A | ENSP00000418775.1:p.Val144Asp | |
| ENST00000493919.5:c.431T>A | ENSP00000418819.1:p.Val144Asp | |
| ENST00000494123.5:c.572T>A | ENSP00000419103.1:p.Val191Asp | |
| ENST00000497488.1:c.-218-2405T>A | ENSP00000418986.1:n.-218-2405T>A | |
| ENST00000586385.5:c.4+27917T>A | ENSP00000465818.1:n.4+27917T>A | |
| ENST00000591534.5:c.-43-22744T>A | ENSP00000467329.1:n.-43-22744T>A | |
| ENST00000591849.5:c.-99+28006T>A | ENSP00000465347.1:n.-99+28006T>A | |
| ENST00000634433.1:c.548-2405T>A | ENSP00000489431.1:n.548-2405T>A | |
| NM_007294.3:c.572T>A , LRG_292t1:c.572T>A | NP_009225.1:p.Val191Asp | |
| NM_007297.3:c.431T>A | NP_009228.2:p.Val144Asp | |
| NM_007298.3:c.572T>A | NP_009229.2:p.Val191Asp | |
| NM_007299.3:c.572T>A | NP_009230.2:p.Val191Asp | |
| NM_007300.3:c.572T>A | NP_009231.2:p.Val191Asp | |
| NR_027676.1:n.708T>A | ||
| NM_007294.4:c.572T>A MANE Select | NP_009225.1:p.Val191Asp | |
| NM_007297.4:c.431T>A | NP_009228.2:p.Val144Asp | |
| NM_007299.4:c.572T>A | NP_009230.2:p.Val191Asp | |
| NM_007300.4:c.572T>A | NP_009231.2:p.Val191Asp | |
| NR_027676.2:n.749T>A |