Linked Data
ClinVar Variation Id:
1795832
ClinVar RCV Id:
RCV002439642
dbSNP Id:
rs376827439
gnomAD v2:
7-117243702-C-A
gnomAD v4:
7-117603648-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117603648C>A , CM000669.2:g.117603648C>A | GRCh38 |
| NC_000007.13:g.117243702C>A , CM000669.1:g.117243702C>A | GRCh37 |
| NC_000007.12:g.117030938C>A | NCBI36 |
| NG_016465.4:g.142865C>A , LRG_663:g.142865C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.2774C>A | ENSP00000497673.2:p.Thr925Asn | |
| ENST00000647978.2:c.*2488C>A | ENSP00000497658.1:n.*2488C>A | |
| ENST00000649781.2:c.2591C>A | ENSP00000497203.1:p.Thr864Asn | |
| ENST00000685018.2:c.2774C>A | ENSP00000510194.2:p.Thr925Asn | |
| ENST00000687278.2:c.2774C>A | ENSP00000509593.2:p.Thr925Asn | |
| ENST00000699585.1:c.2774C>A | ENSP00000514456.1:p.Thr925Asn | |
| ENST00000699598.1:c.2774C>A | ENSP00000514467.1:p.Thr925Asn | |
| ENST00000699599.1:c.2774C>A | ENSP00000514468.1:p.Thr925Asn | |
| ENST00000699600.1:c.2774C>A | ENSP00000514469.1:p.Thr925Asn | |
| ENST00000699601.1:c.*1074C>A | ENSP00000514470.1:n.*1074C>A | |
| ENST00000699602.1:c.2774C>A | ENSP00000514471.1:p.Thr925Asn | |
| ENST00000699604.1:c.*2598C>A | ENSP00000514472.1:n.*2598C>A | |
| ENST00000699605.1:c.2348C>A | ENSP00000514473.1:p.Thr783Asn | |
| ENST00000687278.1:c.365C>A | ENSP00000509593.1:p.Thr122Asn | |
| ENST00000003084.11:c.2774C>A MANE Select | ENSP00000003084.6:p.Thr925Asn | |
| ENST00000647720.1:c.424C>A | ||
| ENST00000648260.1:c.1556C>A | ENSP00000497957.1:p.Thr519Asn | |
| ENST00000649406.1:c.2591C>A | ENSP00000497965.1:p.Thr864Asn | |
| ENST00000649781.1:c.2591C>A | ENSP00000497203.1:p.Thr864Asn | |
| ENST00000003084.10:c.2774C>A | ENSP00000003084.6:p.Thr925Asn | |
| ENST00000426809.5:c.2684C>A | ENSP00000389119.1:p.Thr895Asn | |
| NM_000492.3:c.2774C>A , LRG_663t1:c.2774C>A | NP_000483.3:p.Thr925Asn | |
| XM_011515751.1:c.2864C>A | XP_011514053.1:p.Thr955Asn | |
| XM_011515752.1:c.2864C>A | XP_011514054.1:p.Thr955Asn | |
| XM_011515753.1:c.2531C>A | XP_011514055.1:p.Thr844Asn | |
| XM_011515754.1:c.2531C>A | XP_011514056.1:p.Thr844Asn | |
| NM_000492.4:c.2774C>A MANE Select | NP_000483.3:p.Thr925Asn |