Linked Data
ClinVar Variation Id:
1046906
ClinVar RCV Id:
RCV002242429
dbSNP Id:
rs2059592627
COSMIC:
COSM1349888
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.93758798G>A , CM000672.2:g.93758798G>A | GRCh38 |
| NC_000010.10:g.95518555G>A , CM000672.1:g.95518555G>A | GRCh37 |
| NC_000010.9:g.95508545G>A | NCBI36 |
| NG_011832.1:g.5990G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371418.9:c.254G>A MANE Select | ENSP00000360472.4:p.Gly85Glu | |
| ENST00000635953.1:c.254G>A | ENSP00000490058.1:p.Gly85Glu | |
| ENST00000636140.1:n.39G>A | ||
| ENST00000636155.1:c.254G>A | ENSP00000490355.1:p.Gly85Glu | |
| ENST00000636232.1:c.*40G>A | ENSP00000490325.1:n.*40G>A | |
| ENST00000636683.1:n.9G>A | ||
| ENST00000636754.1:c.*44G>A | ENSP00000489781.1:n.*44G>A | |
| ENST00000636946.1:c.254G>A | ENSP00000490654.1:p.Gly85Glu | |
| ENST00000637037.1:c.254G>A | ENSP00000490860.1:p.Gly85Glu | |
| ENST00000637347.1:n.148+110G>A | ||
| ENST00000637611.1:c.254G>A | ENSP00000489682.1:p.Gly85Glu | |
| ENST00000637689.1:c.-1118G>A | ENSP00000490496.1:n.-1118G>A | |
| ENST00000637925.1:c.254G>A | ENSP00000489763.1:p.Gly85Glu | |
| ENST00000638049.1:c.*12G>A | ENSP00000490597.1:n.*12G>A | |
| ENST00000371413.4:c.254G>A | ENSP00000360467.3:p.Gly85Glu | |
| ENST00000371418.8:c.254G>A | ENSP00000360472.4:p.Gly85Glu | |
| ENST00000478763.2:c.254G>A | ENSP00000486517.1:p.Gly85Glu | |
| ENST00000627420.2:c.*44G>A | ENSP00000487116.1:n.*44G>A | |
| ENST00000627699.1:c.*44G>A | ENSP00000485868.1:n.*44G>A | |
| ENST00000629035.2:c.215+439G>A | ENSP00000486908.1:n.215+439G>A | |
| ENST00000630047.2:c.254G>A | ENSP00000485917.1:p.Gly85Glu | |
| ENST00000630184.2:c.254G>A | ENSP00000486607.1:p.Gly85Glu | |
| ENST00000630487.2:c.*44G>A | ENSP00000486859.1:n.*44G>A | |
| NM_001308275.1:c.254G>A | NP_001295204.1:p.Gly85Glu | |
| NM_001308276.1:c.254G>A | NP_001295205.1:p.Gly85Glu | |
| NM_005097.2:c.254G>A | NP_005088.1:p.Gly85Glu | |
| NM_005097.3:c.254G>A | NP_005088.1:p.Gly85Glu | |
| NR_131777.1:n.599G>A | ||
| XM_017016911.2:c.254G>A | XP_016872400.1:p.Gly85Glu | |
| XM_017016912.2:c.254G>A | XP_016872401.1:p.Gly85Glu | |
| NM_005097.4:c.254G>A MANE Select | NP_005088.1:p.Gly85Glu | |
| NM_001308275.2:c.254G>A | NP_001295204.1:p.Gly85Glu | |
| NM_001308276.2:c.254G>A | NP_001295205.1:p.Gly85Glu | |
| NR_131777.2:n.472G>A |