Linked Data
ClinVar Variation Id:
950626
ClinVar RCV Id:
RCV001222374
dbSNP Id:
rs1597847973
gnomAD v4:
17-43082472-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43082472G>A , CM000679.2:g.43082472G>A | GRCh38 |
| NC_000017.10:g.41234489G>A , CM000679.1:g.41234489G>A | GRCh37 |
| NC_000017.9:g.38488015G>A | NCBI36 |
| NG_005905.2:g.135512C>T , LRG_292:g.135512C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461574.2:c.4289C>T | ENSP00000417241.2:p.Pro1430Leu | |
| ENST00000470026.6:c.4289C>T | ENSP00000419274.2:p.Pro1430Leu | |
| ENST00000473961.6:c.4163C>T | ENSP00000420201.2:p.Pro1388Leu | |
| ENST00000476777.6:c.4283C>T | ENSP00000417554.2:p.Pro1428Leu | |
| ENST00000477152.6:c.4211C>T | ENSP00000419988.2:p.Pro1404Leu | |
| ENST00000478531.6:c.977C>T | ENSP00000420412.2:p.Pro326Leu | |
| ENST00000489037.2:c.4211C>T | ENSP00000420781.2:p.Pro1404Leu | |
| ENST00000493919.6:c.839C>T | ENSP00000418819.2:p.Pro280Leu | |
| ENST00000494123.6:c.4289C>T | ENSP00000419103.2:p.Pro1430Leu | |
| ENST00000497488.2:c.3401C>T | ENSP00000418986.2:p.Pro1134Leu | |
| ENST00000618469.2:c.4289C>T | ENSP00000478114.2:p.Pro1430Leu | |
| ENST00000634433.2:c.4166C>T | ENSP00000489431.2:p.Pro1389Leu | |
| ENST00000644379.2:c.4289C>T | ENSP00000496570.2:p.Pro1430Leu | |
| ENST00000644555.2:c.839C>T | ENSP00000494614.2:p.Pro280Leu | |
| ENST00000652672.2:c.4148C>T | ENSP00000498906.2:p.Pro1383Leu | |
| ENST00000484087.6:c.854C>T | ENSP00000419481.2:p.Pro285Leu | |
| ENST00000700182.1:c.899C>T | ENSP00000514849.1:p.Pro300Leu | |
| ENST00000357654.9:c.4289C>T MANE Select | ENSP00000350283.3:p.Pro1430Leu | |
| ENST00000471181.7:c.4289C>T | ENSP00000418960.2:p.Pro1430Leu | |
| ENST00000644379.1:c.610C>T | ||
| ENST00000352993.7:c.863C>T | ENSP00000312236.5:p.Pro288Leu | |
| ENST00000357654.7:c.4289C>T | ENSP00000350283.3:p.Pro1430Leu | |
| ENST00000461221.5:c.*4072C>T | ENSP00000418548.1:n.*4072C>T | |
| ENST00000461574.1:c.583C>T | ||
| ENST00000468300.5:c.980C>T | ENSP00000417148.1:p.Pro327Leu | |
| ENST00000471181.6:c.4289C>T | ENSP00000418960.2:p.Pro1430Leu | |
| ENST00000478531.5:c.977C>T | ENSP00000420412.1:p.Pro326Leu | |
| ENST00000484087.5:c.602C>T | ENSP00000419481.1:p.Pro201Leu | |
| ENST00000487825.5:c.605C>T | ENSP00000418212.1:p.Pro202Leu | |
| ENST00000491747.6:c.980C>T | ENSP00000420705.2:p.Pro327Leu | |
| ENST00000493795.5:c.4148C>T | ENSP00000418775.1:p.Pro1383Leu | |
| ENST00000493919.5:c.839C>T | ENSP00000418819.1:p.Pro280Leu | |
| ENST00000586385.5:c.5-18521C>T | ENSP00000465818.1:n.5-18521C>T | |
| ENST00000591534.5:c.-43-7951C>T | ENSP00000467329.1:n.-43-7951C>T | |
| ENST00000591849.5:c.-98-32282C>T | ENSP00000465347.1:n.-98-32282C>T | |
| ENST00000621897.1:n.183C>T | ||
| NM_007294.3:c.4289C>T , LRG_292t1:c.4289C>T | NP_009225.1:p.Pro1430Leu | |
| NM_007297.3:c.4148C>T | NP_009228.2:p.Pro1383Leu | |
| NM_007298.3:c.980C>T | NP_009229.2:p.Pro327Leu | |
| NM_007299.3:c.980C>T | NP_009230.2:p.Pro327Leu | |
| NM_007300.3:c.4289C>T | NP_009231.2:p.Pro1430Leu | |
| NR_027676.1:n.4425C>T | ||
| NM_007294.4:c.4289C>T MANE Select | NP_009225.1:p.Pro1430Leu | |
| NM_007297.4:c.4148C>T | NP_009228.2:p.Pro1383Leu | |
| NM_007299.4:c.980C>T | NP_009230.2:p.Pro327Leu | |
| NM_007300.4:c.4289C>T | NP_009231.2:p.Pro1430Leu | |
| NR_027676.2:n.4466C>T |