Linked Data
ClinVar Variation Id:
89064
dbSNP Id:
rs80357075
ExAC:
17:41228579 T / A
gnomAD v2:
17-41228579-T-A
gnomAD v3:
17-43076562-T-A
gnomAD v4:
17-43076562-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43076562T>A , CM000679.2:g.43076562T>A | GRCh38 |
| NC_000017.10:g.41228579T>A , CM000679.1:g.41228579T>A | GRCh37 |
| NC_000017.9:g.38482105T>A | NCBI36 |
| NG_005905.2:g.141422A>T , LRG_292:g.141422A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4407A>T | ENSP00000417241.2:p.Glu1469Asp | |
| ENST00000470026.6:c.4410A>T | ENSP00000419274.2:p.Glu1470Asp | |
| ENST00000473961.6:c.4284A>T | ENSP00000420201.2:p.Glu1428Asp | |
| ENST00000476777.6:c.4404A>T | ENSP00000417554.2:p.Glu1468Asp | |
| ENST00000477152.6:c.4332A>T | ENSP00000419988.2:p.Glu1444Asp | |
| ENST00000478531.6:c.1098A>T | ENSP00000420412.2:p.Glu366Asp | |
| ENST00000489037.2:c.4332A>T | ENSP00000420781.2:p.Glu1444Asp | |
| ENST00000493919.6:c.960A>T | ENSP00000418819.2:p.Glu320Asp | |
| ENST00000494123.6:c.4410A>T | ENSP00000419103.2:p.Glu1470Asp | |
| ENST00000497488.2:c.3522A>T | ENSP00000418986.2:p.Glu1174Asp | |
| ENST00000618469.2:c.4410A>T | ENSP00000478114.2:p.Glu1470Asp | |
| ENST00000634433.2:c.4287A>T | ENSP00000489431.2:p.Glu1429Asp | |
| ENST00000644379.2:c.4476A>T | ENSP00000496570.2:p.Glu1492Asp | |
| ENST00000644555.2:c.960A>T | ENSP00000494614.2:p.Glu320Asp | |
| ENST00000652672.2:c.4269A>T | ENSP00000498906.2:p.Glu1423Asp | |
| ENST00000484087.6:c.972A>T | ENSP00000419481.2:p.Glu324Asp | |
| ENST00000700182.1:c.1017A>T | ENSP00000514849.1:p.Glu339Asp | |
| ENST00000357654.9:c.4410A>T MANE Select | ENSP00000350283.3:p.Glu1470Asp | |
| ENST00000471181.7:c.4473A>T | ENSP00000418960.2:p.Glu1491Asp | |
| ENST00000644379.1:c.797A>T | ||
| ENST00000352993.7:c.984A>T | ENSP00000312236.5:p.Glu328Asp | |
| ENST00000357654.7:c.4410A>T | ENSP00000350283.3:p.Glu1470Asp | |
| ENST00000461221.5:c.*4193A>T | ENSP00000418548.1:n.*4193A>T | |
| ENST00000461574.1:c.701A>T | ||
| ENST00000468300.5:c.1098A>T | ENSP00000417148.1:p.Glu366Asp | |
| ENST00000471181.6:c.4473A>T | ENSP00000418960.2:p.Glu1491Asp | |
| ENST00000478531.5:c.1098A>T | ENSP00000420412.1:p.Glu366Asp | |
| ENST00000484087.5:c.723A>T | ENSP00000419481.1:p.Glu241Asp | |
| ENST00000487825.5:c.726A>T | ENSP00000418212.1:p.Glu242Asp | |
| ENST00000491747.6:c.1098A>T | ENSP00000420705.2:p.Glu366Asp | |
| ENST00000493795.5:c.4269A>T | ENSP00000418775.1:p.Glu1423Asp | |
| ENST00000493919.5:c.960A>T | ENSP00000418819.1:p.Glu320Asp | |
| ENST00000586385.5:c.5-12611A>T | ENSP00000465818.1:n.5-12611A>T | |
| ENST00000591534.5:c.-43-2041A>T | ENSP00000467329.1:n.-43-2041A>T | |
| ENST00000591849.5:c.-98-26372A>T | ENSP00000465347.1:n.-98-26372A>T | |
| ENST00000621897.1:n.301A>T | ||
| NM_007294.3:c.4410A>T , LRG_292t1:c.4410A>T | NP_009225.1:p.Glu1470Asp | |
| NM_007297.3:c.4269A>T | NP_009228.2:p.Glu1423Asp | |
| NM_007298.3:c.1098A>T | NP_009229.2:p.Glu366Asp | |
| NM_007299.3:c.1098A>T | NP_009230.2:p.Glu366Asp | |
| NM_007300.3:c.4473A>T | NP_009231.2:p.Glu1491Asp | |
| NR_027676.1:n.4546A>T | ||
| NM_007294.4:c.4410A>T MANE Select | NP_009225.1:p.Glu1470Asp | |
| NM_007297.4:c.4269A>T | NP_009228.2:p.Glu1423Asp | |
| NM_007299.4:c.1098A>T | NP_009230.2:p.Glu366Asp | |
| NM_007300.4:c.4473A>T | NP_009231.2:p.Glu1491Asp | |
| NR_027676.2:n.4587A>T |