Linked Data
ClinVar Variation Id:
1415627
dbSNP Id:
rs773608087
ExAC:
17:7124281 G / A
gnomAD v2:
17-7124281-G-A
gnomAD v4:
17-7220962-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7220962G>A , CM000679.2:g.7220962G>A | GRCh38 |
| NC_000017.10:g.7124281G>A , CM000679.1:g.7124281G>A | GRCh37 |
| NC_000017.9:g.7065005G>A | NCBI36 |
| NG_007975.1:g.6129G>A | |
| NG_008391.2:g.4089C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.381G>A MANE Select | ENSP00000349297.5:p.Met127Ile | |
| ENST00000322910.9:c.*336G>A | ENSP00000325395.5:n.*336G>A | |
| ENST00000350303.9:c.315G>A | ENSP00000344152.5:p.Met105Ile | |
| ENST00000356839.9:c.381G>A | ENSP00000349297.5:p.Met127Ile | |
| ENST00000543245.6:c.450G>A | ENSP00000438689.2:p.Met150Ile | |
| ENST00000577191.5:n.458G>A | ||
| ENST00000577433.5:n.589G>A | ||
| ENST00000577857.5:n.293+132G>A | ||
| ENST00000579286.5:n.562G>A | ||
| ENST00000579886.2:c.219G>A | ENSP00000463246.1:p.Met73Ile | |
| ENST00000580365.1:n.112G>A | ||
| ENST00000581378.5:c.80G>A | ||
| ENST00000581562.5:n.428G>A | ||
| ENST00000582056.5:n.564G>A | ||
| ENST00000582166.1:n.362G>A | ||
| ENST00000583312.5:c.381G>A | ENSP00000467920.1:p.Met127Ile | |
| ENST00000584103.5:c.414G>A | ENSP00000465353.1:p.Met138Ile | |
| NM_000018.3:c.381G>A | NP_000009.1:p.Met127Ile | |
| NM_001033859.2:c.315G>A | NP_001029031.1:p.Met105Ile | |
| NM_001270447.1:c.450G>A | NP_001257376.1:p.Met150Ile | |
| NM_001270448.1:c.153G>A | NP_001257377.1:p.Met51Ile | |
| XM_006721516.2:c.381G>A | XP_006721579.2:p.Met127Ile | |
| XM_011523829.1:c.381G>A | XP_011522131.1:p.Met127Ile | |
| XM_011523830.1:c.381G>A | XP_011522132.1:p.Met127Ile | |
| XR_934021.1:n.488G>A | ||
| XR_934022.1:n.488G>A | ||
| XR_934023.1:n.488G>A | ||
| XM_006721516.3:c.381G>A | XP_006721579.2:p.Met127Ile | |
| XM_011523829.2:c.381G>A | XP_011522131.1:p.Met127Ile | |
| XM_011523830.2:c.381G>A | XP_011522132.1:p.Met127Ile | |
| XM_024450741.1:c.381G>A | XP_024306509.1:p.Met127Ile | |
| XR_934021.2:n.440G>A | ||
| XR_934022.2:n.440G>A | ||
| XR_934023.2:n.440G>A | ||
| NM_000018.4:c.381G>A MANE Select | NP_000009.1:p.Met127Ile | |
| NM_001033859.3:c.315G>A | NP_001029031.1:p.Met105Ile | |
| NM_001270447.2:c.450G>A | NP_001257376.1:p.Met150Ile | |
| NM_001270448.2:c.153G>A | NP_001257377.1:p.Met51Ile |