Linked Data
ClinVar Variation Id:
1998578
ClinVar RCV Id:
RCV002810558
MyVariant Identifiers:
chr17:g.7127834G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224515G>A , CM000679.2:g.7224515G>A | GRCh38 |
| NC_000017.10:g.7127834G>A , CM000679.1:g.7127834G>A | GRCh37 |
| NC_000017.9:g.7068558G>A | NCBI36 |
| NG_007975.1:g.9682G>A | |
| NG_008391.2:g.536C>T | |
| NG_033038.1:g.15030C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1641G>A MANE Select | ENSP00000349297.5:p.Val547= | |
| ENST00000322910.9:c.*1596G>A | ENSP00000325395.5:n.*1596G>A | |
| ENST00000350303.9:c.1575G>A | ENSP00000344152.5:p.Val525= | |
| ENST00000356839.9:c.1641G>A | ENSP00000349297.5:p.Val547= | |
| ENST00000542255.6:c.499G>A | ||
| ENST00000543245.6:c.1710G>A | ENSP00000438689.2:p.Val570= | |
| ENST00000578319.5:n.222G>A | ||
| ENST00000578711.1:n.1011G>A | ||
| ENST00000578809.5:n.213G>A | ||
| ENST00000579391.1:n.245G>A | ||
| ENST00000579425.5:n.757G>A | ||
| ENST00000579546.1:c.376G>A | ||
| ENST00000579894.5:n.428G>A | ||
| ENST00000582450.1:n.149G>A | ||
| ENST00000583074.5:n.262G>A | ||
| ENST00000583848.5:c.27G>A | ENSP00000466487.1:p.Val9= | |
| ENST00000583850.5:n.412G>A | ||
| ENST00000583858.5:c.572G>A | ||
| ENST00000585203.6:n.832G>A | ||
| NM_000018.3:c.1641G>A | NP_000009.1:p.Val547= | |
| NM_001033859.2:c.1575G>A | NP_001029031.1:p.Val525= | |
| NM_001270447.1:c.1710G>A | NP_001257376.1:p.Val570= | |
| NM_001270448.1:c.1413G>A | NP_001257377.1:p.Val471= | |
| XM_006721516.2:c.1641G>A | XP_006721579.2:p.Val547= | |
| XM_011523829.1:c.1539G>A | XP_011522131.1:p.Val513= | |
| XM_011523830.1:c.1539G>A | XP_011522132.1:p.Val513= | |
| XR_934021.1:n.1744G>A | ||
| XR_934022.1:n.1650G>A | ||
| XR_934023.1:n.1650G>A | ||
| XM_006721516.3:c.1641G>A | XP_006721579.2:p.Val547= | |
| XM_011523829.2:c.1539G>A | XP_011522131.1:p.Val513= | |
| XM_011523830.2:c.1539G>A | XP_011522132.1:p.Val513= | |
| XM_024450741.1:c.1629G>A | XP_024306509.1:p.Val543= | |
| XR_934021.2:n.1696G>A | ||
| XR_934022.2:n.1602G>A | ||
| XR_934023.2:n.1602G>A | ||
| NM_000018.4:c.1641G>A MANE Select | NP_000009.1:p.Val547= | |
| NM_001033859.3:c.1575G>A | NP_001029031.1:p.Val525= | |
| NM_001270447.2:c.1710G>A | NP_001257376.1:p.Val570= | |
| NM_001270448.2:c.1413G>A | NP_001257377.1:p.Val471= |