Linked Data
ClinVar Variation Id:
2586859
ClinVar RCV Id:
RCV003358431
dbSNP Id:
rs1427020869
gnomAD v2:
11-67257805-G-A
gnomAD v4:
11-67490334-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67490334G>A , CM000673.2:g.67490334G>A | GRCh38 |
| NC_000011.9:g.67257805G>A , CM000673.1:g.67257805G>A | GRCh37 |
| NC_000011.8:g.67014381G>A | NCBI36 |
| NG_008969.1:g.12301G>A , LRG_460:g.12301G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000525341.2:c.641G>A | ||
| ENST00000528641.7:c.475G>A | ENSP00000434982.3:p.Glu159Lys | |
| ENST00000529797.2:n.1176G>A | ||
| ENST00000682324.1:c.469-663G>A | ENSP00000508017.1:n.469-663G>A | |
| ENST00000682659.1:c.295G>A | ENSP00000507351.1:p.Glu99Lys | |
| ENST00000682699.1:c.664G>A | ENSP00000507935.1:p.Glu222Lys | |
| ENST00000683237.1:c.664G>A | ENSP00000507343.1:p.Glu222Lys | |
| ENST00000683856.1:c.487G>A | ENSP00000507979.1:p.Glu163Lys | |
| ENST00000684006.1:c.664G>A | ENSP00000507269.1:p.Glu222Lys | |
| ENST00000684657.1:c.484G>A | ENSP00000507961.1:p.Glu162Lys | |
| ENST00000279146.8:c.664G>A MANE Select | ENSP00000279146.3:p.Glu222Lys | |
| ENST00000279146.7:c.664G>A | ENSP00000279146.3:p.Glu222Lys | |
| ENST00000525341.1:c.316G>A | ENSP00000476993.1:p.Glu106Lys | |
| ENST00000528641.6:c.475G>A | ENSP00000434982.2:p.Glu159Lys | |
| NM_001302959.1:c.487G>A | NP_001289888.1:p.Glu163Lys | |
| NM_001302960.1:c.664G>A | NP_001289889.1:p.Glu222Lys | |
| NM_003977.3:c.664G>A | NP_003968.3:p.Glu222Lys | |
| XM_024448761.1:c.664G>A | XP_024304529.1:p.Glu222Lys | |
| NM_003977.4:c.664G>A MANE Select | NP_003968.3:p.Glu222Lys | |
| NM_001302960.2:c.664G>A | NP_001289889.1:p.Glu222Lys | |
| NM_001302959.2:c.487G>A | NP_001289888.1:p.Glu163Lys |