Linked Data
ClinVar Variation Id:
224433
dbSNP Id:
rs876658221
gnomAD v2:
17-41242987-A-G
gnomAD v4:
17-43090970-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43090970A>G , CM000679.2:g.43090970A>G | GRCh38 |
| NC_000017.10:g.41242987A>G , CM000679.1:g.41242987A>G | GRCh37 |
| NC_000017.9:g.38496513A>G | NCBI36 |
| NG_005905.2:g.127014T>C , LRG_292:g.127014T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4159T>C | ENSP00000417241.2:p.Ser1387Pro | |
| ENST00000470026.6:c.4159T>C | ENSP00000419274.2:p.Ser1387Pro | |
| ENST00000473961.6:c.4033T>C | ENSP00000420201.2:p.Ser1345Pro | |
| ENST00000476777.6:c.4156T>C | ENSP00000417554.2:p.Ser1386Pro | |
| ENST00000477152.6:c.4081T>C | ENSP00000419988.2:p.Ser1361Pro | |
| ENST00000478531.6:c.847T>C | ENSP00000420412.2:p.Ser283Pro | |
| ENST00000489037.2:c.4081T>C | ENSP00000420781.2:p.Ser1361Pro | |
| ENST00000493919.6:c.709T>C | ENSP00000418819.2:p.Ser237Pro | |
| ENST00000494123.6:c.4159T>C | ENSP00000419103.2:p.Ser1387Pro | |
| ENST00000497488.2:c.3271T>C | ENSP00000418986.2:p.Ser1091Pro | |
| ENST00000618469.2:c.4159T>C | ENSP00000478114.2:p.Ser1387Pro | |
| ENST00000634433.2:c.4036T>C | ENSP00000489431.2:p.Ser1346Pro | |
| ENST00000644379.2:c.4159T>C | ENSP00000496570.2:p.Ser1387Pro | |
| ENST00000644555.2:c.709T>C | ENSP00000494614.2:p.Ser237Pro | |
| ENST00000652672.2:c.4018T>C | ENSP00000498906.2:p.Ser1340Pro | |
| ENST00000484087.6:c.727T>C | ENSP00000419481.2:p.Ser243Pro | |
| ENST00000700182.1:c.769T>C | ENSP00000514849.1:p.Ser257Pro | |
| ENST00000357654.9:c.4159T>C MANE Select | ENSP00000350283.3:p.Ser1387Pro | |
| ENST00000471181.7:c.4159T>C | ENSP00000418960.2:p.Ser1387Pro | |
| ENST00000644379.1:c.480T>C | ||
| ENST00000352993.7:c.733T>C | ENSP00000312236.5:p.Ser245Pro | |
| ENST00000357654.7:c.4159T>C | ENSP00000350283.3:p.Ser1387Pro | |
| ENST00000461221.5:c.*3942T>C | ENSP00000418548.1:n.*3942T>C | |
| ENST00000461574.1:c.453T>C | ||
| ENST00000468300.5:c.850T>C | ENSP00000417148.1:p.Ser284Pro | |
| ENST00000471181.6:c.4159T>C | ENSP00000418960.2:p.Ser1387Pro | |
| ENST00000478531.5:c.847T>C | ENSP00000420412.1:p.Ser283Pro | |
| ENST00000484087.5:c.472T>C | ENSP00000419481.1:p.Ser158Pro | |
| ENST00000487825.5:c.475T>C | ENSP00000418212.1:p.Ser159Pro | |
| ENST00000491747.6:c.850T>C | ENSP00000420705.2:p.Ser284Pro | |
| ENST00000493795.5:c.4018T>C | ENSP00000418775.1:p.Ser1340Pro | |
| ENST00000493919.5:c.709T>C | ENSP00000418819.1:p.Ser237Pro | |
| ENST00000586385.5:c.5-27019T>C | ENSP00000465818.1:n.5-27019T>C | |
| ENST00000591534.5:c.-43-16449T>C | ENSP00000467329.1:n.-43-16449T>C | |
| ENST00000591849.5:c.-99+34301T>C | ENSP00000465347.1:n.-99+34301T>C | |
| NM_007294.3:c.4159T>C , LRG_292t1:c.4159T>C | NP_009225.1:p.Ser1387Pro | |
| NM_007297.3:c.4018T>C | NP_009228.2:p.Ser1340Pro | |
| NM_007298.3:c.850T>C | NP_009229.2:p.Ser284Pro | |
| NM_007299.3:c.850T>C | NP_009230.2:p.Ser284Pro | |
| NM_007300.3:c.4159T>C | NP_009231.2:p.Ser1387Pro | |
| NR_027676.1:n.4295T>C | ||
| NM_007294.4:c.4159T>C MANE Select | NP_009225.1:p.Ser1387Pro | |
| NM_007297.4:c.4018T>C | NP_009228.2:p.Ser1340Pro | |
| NM_007299.4:c.850T>C | NP_009230.2:p.Ser284Pro | |
| NM_007300.4:c.4159T>C | NP_009231.2:p.Ser1387Pro | |
| NR_027676.2:n.4336T>C |