Linked Data
ClinVar Variation Id:
521398
dbSNP Id:
rs758737171
ExAC:
7:44184809 C / T
gnomAD v2:
7-44184809-C-T
gnomAD v3:
7-44145210-C-T
gnomAD v4:
7-44145210-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.44145210C>T , CM000669.2:g.44145210C>T | GRCh38 |
| NC_000007.13:g.44184809C>T , CM000669.1:g.44184809C>T | GRCh37 |
| NC_000007.12:g.44151334C>T | NCBI36 |
| NG_008847.1:g.49214G>A | |
| NG_008847.2:g.57961G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395796.8:c.*1322G>A | ENSP00000379142.4:n.*1322G>A | |
| ENST00000616242.5:c.*444G>A | ENSP00000482149.2:n.*444G>A | |
| ENST00000683378.1:n.550G>A | ||
| ENST00000336642.9:c.358G>A | ENSP00000338009.5:p.Glu120Lys | |
| ENST00000345378.7:c.1327G>A | ENSP00000223366.2:p.Glu443Lys | |
| ENST00000403799.8:c.1324G>A MANE Select | ENSP00000384247.3:p.Glu442Lys | |
| ENST00000671824.1:c.1387G>A | ENSP00000500264.1:p.Glu463Lys | |
| ENST00000672743.1:n.336G>A | ||
| ENST00000673284.1:c.1324G>A | ENSP00000499852.1:p.Glu442Lys | |
| ENST00000336642.8:c.376G>A | ENSP00000338009.4:p.Glu126Lys | |
| ENST00000345378.6:c.1327G>A | ENSP00000223366.2:p.Glu443Lys | |
| ENST00000395796.7:c.1321G>A | ENSP00000379142.3:p.Glu441Lys | |
| ENST00000403799.7:c.1324G>A | ENSP00000384247.3:p.Glu442Lys | |
| ENST00000437084.1:c.1273G>A | ENSP00000402840.1:p.Glu425Lys | |
| ENST00000459642.1:n.704G>A | ||
| ENST00000616242.4:c.1321G>A | ENSP00000482149.1:p.Glu441Lys | |
| NM_000162.3:c.1324G>A | NP_000153.1:p.Glu442Lys | |
| NM_033507.1:c.1327G>A | NP_277042.1:p.Glu443Lys | |
| NM_033508.1:c.1321G>A | NP_277043.1:p.Glu441Lys | |
| NM_000162.4:c.1324G>A | NP_000153.1:p.Glu442Lys | |
| NM_001354800.1:c.1324G>A | NP_001341729.1:p.Glu442Lys | |
| NM_001354801.1:c.313G>A | NP_001341730.1:p.Glu105Lys | |
| NM_001354802.1:c.184G>A | NP_001341731.1:p.Glu62Lys | |
| NM_001354803.1:c.358G>A | NP_001341732.1:p.Glu120Lys | |
| NM_033507.2:c.1327G>A | NP_277042.1:p.Glu443Lys | |
| NM_033508.2:c.1321G>A | NP_277043.1:p.Glu441Lys | |
| XM_024446707.1:c.184G>A | XP_024302475.1:p.Glu62Lys | |
| NM_000162.5:c.1324G>A MANE Select | NP_000153.1:p.Glu442Lys | |
| NM_033507.3:c.1327G>A | NP_277042.1:p.Glu443Lys | |
| NM_033508.3:c.1321G>A | NP_277043.1:p.Glu441Lys | |
| NM_001354803.2:c.358G>A | NP_001341732.1:p.Glu120Lys |