Linked Data
ClinVar Variation Id:
594285
dbSNP Id:
rs779569793
ExAC:
7:117243823 C / A
gnomAD v2:
7-117243823-C-A
gnomAD v3:
7-117603769-C-A
gnomAD v4:
7-117603769-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117603769C>A , CM000669.2:g.117603769C>A | GRCh38 |
| NC_000007.13:g.117243823C>A , CM000669.1:g.117243823C>A | GRCh37 |
| NC_000007.12:g.117031059C>A | NCBI36 |
| NG_016465.4:g.142986C>A , LRG_663:g.142986C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.2895C>A | ENSP00000497673.2:p.Asn965Lys | |
| ENST00000647978.2:c.*2609C>A | ENSP00000497658.1:n.*2609C>A | |
| ENST00000649781.2:c.2712C>A | ENSP00000497203.1:p.Asn904Lys | |
| ENST00000685018.2:c.2895C>A | ENSP00000510194.2:p.Asn965Lys | |
| ENST00000687278.2:c.2895C>A | ENSP00000509593.2:p.Asn965Lys | |
| ENST00000699585.1:c.2895C>A | ENSP00000514456.1:p.Asn965Lys | |
| ENST00000699598.1:c.2895C>A | ENSP00000514467.1:p.Asn965Lys | |
| ENST00000699599.1:c.2895C>A | ENSP00000514468.1:p.Asn965Lys | |
| ENST00000699600.1:c.2895C>A | ENSP00000514469.1:p.Asn965Lys | |
| ENST00000699601.1:c.*1195C>A | ENSP00000514470.1:n.*1195C>A | |
| ENST00000699602.1:c.2895C>A | ENSP00000514471.1:p.Asn965Lys | |
| ENST00000699604.1:c.*2719C>A | ENSP00000514472.1:n.*2719C>A | |
| ENST00000699605.1:c.2469C>A | ENSP00000514473.1:p.Asn823Lys | |
| ENST00000687278.1:c.486C>A | ENSP00000509593.1:p.Asn162Lys | |
| ENST00000003084.11:c.2895C>A MANE Select | ENSP00000003084.6:p.Asn965Lys | |
| ENST00000647720.1:c.545C>A | ||
| ENST00000648260.1:c.1677C>A | ENSP00000497957.1:p.Asn559Lys | |
| ENST00000649406.1:c.2712C>A | ENSP00000497965.1:p.Asn904Lys | |
| ENST00000649781.1:c.2712C>A | ENSP00000497203.1:p.Asn904Lys | |
| ENST00000003084.10:c.2895C>A | ENSP00000003084.6:p.Asn965Lys | |
| ENST00000426809.5:c.2805C>A | ENSP00000389119.1:p.Asn935Lys | |
| NM_000492.3:c.2895C>A , LRG_663t1:c.2895C>A | NP_000483.3:p.Asn965Lys | |
| XM_011515751.1:c.2985C>A | XP_011514053.1:p.Asn995Lys | |
| XM_011515752.1:c.2985C>A | XP_011514054.1:p.Asn995Lys | |
| XM_011515753.1:c.2652C>A | XP_011514055.1:p.Asn884Lys | |
| XM_011515754.1:c.2652C>A | XP_011514056.1:p.Asn884Lys | |
| NM_000492.4:c.2895C>A MANE Select | NP_000483.3:p.Asn965Lys |