Linked Data
ClinVar Variation Id:
17676
dbSNP Id:
rs41293455
ExAC:
17:41234451 G / C
gnomAD v2:
17-41234451-G-C
gnomAD v3:
17-43082434-G-C
gnomAD v4:
17-43082434-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43082434G>C , CM000679.2:g.43082434G>C | GRCh38 |
| NC_000017.10:g.41234451G>C , CM000679.1:g.41234451G>C | GRCh37 |
| NC_000017.9:g.38487977G>C | NCBI36 |
| NG_005905.2:g.135550C>G , LRG_292:g.135550C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461574.2:c.4327C>G | ENSP00000417241.2:p.Arg1443Gly | |
| ENST00000470026.6:c.4327C>G | ENSP00000419274.2:p.Arg1443Gly | |
| ENST00000473961.6:c.4201C>G | ENSP00000420201.2:p.Arg1401Gly | |
| ENST00000476777.6:c.4321C>G | ENSP00000417554.2:p.Arg1441Gly | |
| ENST00000477152.6:c.4249C>G | ENSP00000419988.2:p.Arg1417Gly | |
| ENST00000478531.6:c.1015C>G | ENSP00000420412.2:p.Arg339Gly | |
| ENST00000489037.2:c.4249C>G | ENSP00000420781.2:p.Arg1417Gly | |
| ENST00000493919.6:c.877C>G | ENSP00000418819.2:p.Arg293Gly | |
| ENST00000494123.6:c.4327C>G | ENSP00000419103.2:p.Arg1443Gly | |
| ENST00000497488.2:c.3439C>G | ENSP00000418986.2:p.Arg1147Gly | |
| ENST00000618469.2:c.4327C>G | ENSP00000478114.2:p.Arg1443Gly | |
| ENST00000634433.2:c.4204C>G | ENSP00000489431.2:p.Arg1402Gly | |
| ENST00000644379.2:c.4327C>G | ENSP00000496570.2:p.Arg1443Gly | |
| ENST00000644555.2:c.877C>G | ENSP00000494614.2:p.Arg293Gly | |
| ENST00000652672.2:c.4186C>G | ENSP00000498906.2:p.Arg1396Gly | |
| ENST00000484087.6:c.892C>G | ENSP00000419481.2:p.Arg298Gly | |
| ENST00000700182.1:c.937C>G | ENSP00000514849.1:p.Arg313Gly | |
| ENST00000357654.9:c.4327C>G MANE Select | ENSP00000350283.3:p.Arg1443Gly | |
| ENST00000471181.7:c.4327C>G | ENSP00000418960.2:p.Arg1443Gly | |
| ENST00000644379.1:c.648C>G | ||
| ENST00000352993.7:c.901C>G | ENSP00000312236.5:p.Arg301Gly | |
| ENST00000357654.7:c.4327C>G | ENSP00000350283.3:p.Arg1443Gly | |
| ENST00000461221.5:c.*4110C>G | ENSP00000418548.1:n.*4110C>G | |
| ENST00000461574.1:c.621C>G | ||
| ENST00000468300.5:c.1018C>G | ENSP00000417148.1:p.Arg340Gly | |
| ENST00000471181.6:c.4327C>G | ENSP00000418960.2:p.Arg1443Gly | |
| ENST00000478531.5:c.1015C>G | ENSP00000420412.1:p.Arg339Gly | |
| ENST00000484087.5:c.640C>G | ENSP00000419481.1:p.Arg214Gly | |
| ENST00000487825.5:c.643C>G | ENSP00000418212.1:p.Arg215Gly | |
| ENST00000491747.6:c.1018C>G | ENSP00000420705.2:p.Arg340Gly | |
| ENST00000493795.5:c.4186C>G | ENSP00000418775.1:p.Arg1396Gly | |
| ENST00000493919.5:c.877C>G | ENSP00000418819.1:p.Arg293Gly | |
| ENST00000586385.5:c.5-18483C>G | ENSP00000465818.1:n.5-18483C>G | |
| ENST00000591534.5:c.-43-7913C>G | ENSP00000467329.1:n.-43-7913C>G | |
| ENST00000591849.5:c.-98-32244C>G | ENSP00000465347.1:n.-98-32244C>G | |
| ENST00000621897.1:n.221C>G | ||
| NM_007294.3:c.4327C>G , LRG_292t1:c.4327C>G | NP_009225.1:p.Arg1443Gly | |
| NM_007297.3:c.4186C>G | NP_009228.2:p.Arg1396Gly | |
| NM_007298.3:c.1018C>G | NP_009229.2:p.Arg340Gly | |
| NM_007299.3:c.1018C>G | NP_009230.2:p.Arg340Gly | |
| NM_007300.3:c.4327C>G | NP_009231.2:p.Arg1443Gly | |
| NR_027676.1:n.4463C>G | ||
| NM_007294.4:c.4327C>G MANE Select | NP_009225.1:p.Arg1443Gly | |
| NM_007297.4:c.4186C>G | NP_009228.2:p.Arg1396Gly | |
| NM_007299.4:c.1018C>G | NP_009230.2:p.Arg340Gly | |
| NM_007300.4:c.4327C>G | NP_009231.2:p.Arg1443Gly | |
| NR_027676.2:n.4504C>G |