Linked Data
dbSNP Id:
rs397508550
gnomAD v2:
7-117254688-G-A
gnomAD v3:
7-117614634-G-A
gnomAD v4:
7-117614634-G-A
COSMIC:
COSM5871660
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117614634G>A , CM000669.2:g.117614634G>A | GRCh38 |
| NC_000007.13:g.117254688G>A , CM000669.1:g.117254688G>A | GRCh37 |
| NC_000007.12:g.117041924G>A | NCBI36 |
| NG_016465.4:g.153851G>A , LRG_663:g.153851G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.3389G>A | ENSP00000497673.2:p.Gly1130Asp | |
| ENST00000647978.2:c.*3103G>A | ENSP00000497658.1:n.*3103G>A | |
| ENST00000649781.2:c.3206G>A | ENSP00000497203.1:p.Gly1069Asp | |
| ENST00000685018.2:c.3389G>A | ENSP00000510194.2:p.Gly1130Asp | |
| ENST00000687278.2:c.3389G>A | ENSP00000509593.2:p.Gly1130Asp | |
| ENST00000699585.1:c.3389G>A | ENSP00000514456.1:p.Gly1130Asp | |
| ENST00000699598.1:c.3389G>A | ENSP00000514467.1:p.Gly1130Asp | |
| ENST00000699599.1:c.3389G>A | ENSP00000514468.1:p.Gly1130Asp | |
| ENST00000699600.1:c.3389G>A | ENSP00000514469.1:p.Gly1130Asp | |
| ENST00000699601.1:c.*1764G>A | ENSP00000514470.1:n.*1764G>A | |
| ENST00000699602.1:c.3383G>A | ENSP00000514471.1:p.Gly1128Asp | |
| ENST00000699604.1:c.*3213G>A | ENSP00000514472.1:n.*3213G>A | |
| ENST00000699605.1:c.2963G>A | ENSP00000514473.1:p.Gly988Asp | |
| ENST00000685018.1:c.137G>A | ENSP00000510194.1:p.Gly46Asp | |
| ENST00000687278.1:c.980G>A | ENSP00000509593.1:p.Gly327Asp | |
| ENST00000003084.11:c.3389G>A MANE Select | ENSP00000003084.6:p.Gly1130Asp | |
| ENST00000647720.1:c.1039G>A | ||
| ENST00000648260.1:c.2171G>A | ENSP00000497957.1:p.Gly724Asp | |
| ENST00000649406.1:c.3206G>A | ENSP00000497965.1:p.Gly1069Asp | |
| ENST00000649781.1:c.3206G>A | ENSP00000497203.1:p.Gly1069Asp | |
| ENST00000003084.10:c.3389G>A | ENSP00000003084.6:p.Gly1130Asp | |
| ENST00000426809.5:c.3299G>A | ENSP00000389119.1:p.Gly1100Asp | |
| ENST00000468795.1:c.214G>A | ||
| NM_000492.3:c.3389G>A , LRG_663t1:c.3389G>A | NP_000483.3:p.Gly1130Asp | |
| XM_011515751.1:c.3479G>A | XP_011514053.1:p.Gly1160Asp | |
| XM_011515752.1:c.3479G>A | XP_011514054.1:p.Gly1160Asp | |
| XM_011515753.1:c.3146G>A | XP_011514055.1:p.Gly1049Asp | |
| XM_011515754.1:c.3146G>A | XP_011514056.1:p.Gly1049Asp | |
| NM_000492.4:c.3389G>A MANE Select | NP_000483.3:p.Gly1130Asp |