Linked Data
ClinVar Variation Id:
1133593
ClinVar RCV Id:
RCV001468223
dbSNP Id:
rs1792456177
gnomAD v3:
7-117614644-G-A
gnomAD v4:
7-117614644-G-A
MyVariant Identifiers:
chr7:g.117254698G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117614644G>A , CM000669.2:g.117614644G>A | GRCh38 |
| NC_000007.13:g.117254698G>A , CM000669.1:g.117254698G>A | GRCh37 |
| NC_000007.12:g.117041934G>A | NCBI36 |
| NG_016465.4:g.153861G>A , LRG_663:g.153861G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.3399G>A | ENSP00000497673.2:p.Leu1133= | |
| ENST00000647978.2:c.*3113G>A | ENSP00000497658.1:n.*3113G>A | |
| ENST00000649781.2:c.3216G>A | ENSP00000497203.1:p.Leu1072= | |
| ENST00000685018.2:c.3399G>A | ENSP00000510194.2:p.Leu1133= | |
| ENST00000687278.2:c.3399G>A | ENSP00000509593.2:p.Leu1133= | |
| ENST00000699585.1:c.3399G>A | ENSP00000514456.1:p.Leu1133= | |
| ENST00000699598.1:c.3399G>A | ENSP00000514467.1:p.Leu1133= | |
| ENST00000699599.1:c.3399G>A | ENSP00000514468.1:p.Leu1133= | |
| ENST00000699600.1:c.3399G>A | ENSP00000514469.1:p.Leu1133= | |
| ENST00000699601.1:c.*1774G>A | ENSP00000514470.1:n.*1774G>A | |
| ENST00000699602.1:c.3393G>A | ENSP00000514471.1:p.Leu1131= | |
| ENST00000699604.1:c.*3223G>A | ENSP00000514472.1:n.*3223G>A | |
| ENST00000699605.1:c.2973G>A | ENSP00000514473.1:p.Leu991= | |
| ENST00000685018.1:c.147G>A | ENSP00000510194.1:p.Leu49= | |
| ENST00000687278.1:c.990G>A | ENSP00000509593.1:p.Leu330= | |
| ENST00000003084.11:c.3399G>A MANE Select | ENSP00000003084.6:p.Leu1133= | |
| ENST00000647720.1:c.1049G>A | ||
| ENST00000648260.1:c.2181G>A | ENSP00000497957.1:p.Leu727= | |
| ENST00000649406.1:c.3216G>A | ENSP00000497965.1:p.Leu1072= | |
| ENST00000649781.1:c.3216G>A | ENSP00000497203.1:p.Leu1072= | |
| ENST00000003084.10:c.3399G>A | ENSP00000003084.6:p.Leu1133= | |
| ENST00000426809.5:c.3309G>A | ENSP00000389119.1:p.Leu1103= | |
| ENST00000468795.1:c.224G>A | ||
| NM_000492.3:c.3399G>A , LRG_663t1:c.3399G>A | NP_000483.3:p.Leu1133= | |
| XM_011515751.1:c.3489G>A | XP_011514053.1:p.Leu1163= | |
| XM_011515752.1:c.3489G>A | XP_011514054.1:p.Leu1163= | |
| XM_011515753.1:c.3156G>A | XP_011514055.1:p.Leu1052= | |
| XM_011515754.1:c.3156G>A | XP_011514056.1:p.Leu1052= | |
| NM_000492.4:c.3399G>A MANE Select | NP_000483.3:p.Leu1133= |