Linked Data
ClinVar Variation Id:
1163408
dbSNP Id:
rs1363658463
gnomAD v2:
17-7127642-G-A
gnomAD v3:
17-7224323-G-A
gnomAD v4:
17-7224323-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224323G>A , CM000679.2:g.7224323G>A | GRCh38 |
| NC_000017.10:g.7127642G>A , CM000679.1:g.7127642G>A | GRCh37 |
| NC_000017.9:g.7068366G>A | NCBI36 |
| NG_007975.1:g.9490G>A | |
| NG_008391.2:g.728C>T | |
| NG_033038.1:g.15222C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1535G>A MANE Select | ENSP00000349297.5:p.Arg512Gln | |
| ENST00000322910.9:c.*1490G>A | ENSP00000325395.5:n.*1490G>A | |
| ENST00000350303.9:c.1469G>A | ENSP00000344152.5:p.Arg490Gln | |
| ENST00000356839.9:c.1535G>A | ENSP00000349297.5:p.Arg512Gln | |
| ENST00000542255.6:c.393G>A | ||
| ENST00000543245.6:c.1604G>A | ENSP00000438689.2:p.Arg535Gln | |
| ENST00000578319.5:n.30G>A | ||
| ENST00000578711.1:n.819G>A | ||
| ENST00000578809.5:n.107G>A | ||
| ENST00000579391.1:n.143G>A | ||
| ENST00000579425.5:n.651G>A | ||
| ENST00000579546.1:c.274G>A | ||
| ENST00000579894.5:n.322G>A | ||
| ENST00000582450.1:n.43G>A | ||
| ENST00000583074.5:n.156G>A | ||
| ENST00000583850.5:n.310G>A | ||
| ENST00000583858.5:c.466G>A | ||
| ENST00000585203.6:n.726G>A | ||
| NM_000018.3:c.1535G>A | NP_000009.1:p.Arg512Gln | |
| NM_001033859.2:c.1469G>A | NP_001029031.1:p.Arg490Gln | |
| NM_001270447.1:c.1604G>A | NP_001257376.1:p.Arg535Gln | |
| NM_001270448.1:c.1307G>A | NP_001257377.1:p.Arg436Gln | |
| XM_006721516.2:c.1535G>A | XP_006721579.2:p.Arg512Gln | |
| XM_011523829.1:c.1437G>A | XP_011522131.1:p.Ala479= | |
| XM_011523830.1:c.1437G>A | XP_011522132.1:p.Ala479= | |
| XR_934021.1:n.1642G>A | ||
| XR_934022.1:n.1544G>A | ||
| XR_934023.1:n.1544G>A | ||
| XM_006721516.3:c.1535G>A | XP_006721579.2:p.Arg512Gln | |
| XM_011523829.2:c.1437G>A | XP_011522131.1:p.Ala479= | |
| XM_011523830.2:c.1437G>A | XP_011522132.1:p.Ala479= | |
| XM_024450741.1:c.1437G>A | XP_024306509.1:p.Ala479= | |
| XR_934021.2:n.1594G>A | ||
| XR_934022.2:n.1496G>A | ||
| XR_934023.2:n.1496G>A | ||
| NM_000018.4:c.1535G>A MANE Select | NP_000009.1:p.Arg512Gln | |
| NM_001033859.3:c.1469G>A | NP_001029031.1:p.Arg490Gln | |
| NM_001270447.2:c.1604G>A | NP_001257376.1:p.Arg535Gln | |
| NM_001270448.2:c.1307G>A | NP_001257377.1:p.Arg436Gln |