Linked Data
ClinVar Variation Id:
1371238
ClinVar RCV Id:
RCV001864484
dbSNP Id:
rs2116096247
gnomAD v4:
7-117614630-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117614630G>C , CM000669.2:g.117614630G>C | GRCh38 |
| NC_000007.13:g.117254684G>C , CM000669.1:g.117254684G>C | GRCh37 |
| NC_000007.12:g.117041920G>C | NCBI36 |
| NG_016465.4:g.153847G>C , LRG_663:g.153847G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647720.2:c.3385G>C | ENSP00000497673.2:p.Val1129Leu | |
| ENST00000647978.2:c.*3099G>C | ENSP00000497658.1:n.*3099G>C | |
| ENST00000649781.2:c.3202G>C | ENSP00000497203.1:p.Val1068Leu | |
| ENST00000685018.2:c.3385G>C | ENSP00000510194.2:p.Val1129Leu | |
| ENST00000687278.2:c.3385G>C | ENSP00000509593.2:p.Val1129Leu | |
| ENST00000699585.1:c.3385G>C | ENSP00000514456.1:p.Val1129Leu | |
| ENST00000699598.1:c.3385G>C | ENSP00000514467.1:p.Val1129Leu | |
| ENST00000699599.1:c.3385G>C | ENSP00000514468.1:p.Val1129Leu | |
| ENST00000699600.1:c.3385G>C | ENSP00000514469.1:p.Val1129Leu | |
| ENST00000699601.1:c.*1760G>C | ENSP00000514470.1:n.*1760G>C | |
| ENST00000699602.1:c.3379G>C | ENSP00000514471.1:p.Val1127Leu | |
| ENST00000699604.1:c.*3209G>C | ENSP00000514472.1:n.*3209G>C | |
| ENST00000699605.1:c.2959G>C | ENSP00000514473.1:p.Val987Leu | |
| ENST00000685018.1:c.133G>C | ENSP00000510194.1:p.Val45Leu | |
| ENST00000687278.1:c.976G>C | ENSP00000509593.1:p.Val326Leu | |
| ENST00000003084.11:c.3385G>C MANE Select | ENSP00000003084.6:p.Val1129Leu | |
| ENST00000647720.1:c.1035G>C | ||
| ENST00000648260.1:c.2167G>C | ENSP00000497957.1:p.Val723Leu | |
| ENST00000649406.1:c.3202G>C | ENSP00000497965.1:p.Val1068Leu | |
| ENST00000649781.1:c.3202G>C | ENSP00000497203.1:p.Val1068Leu | |
| ENST00000003084.10:c.3385G>C | ENSP00000003084.6:p.Val1129Leu | |
| ENST00000426809.5:c.3295G>C | ENSP00000389119.1:p.Val1099Leu | |
| ENST00000468795.1:c.210G>C | ||
| NM_000492.3:c.3385G>C , LRG_663t1:c.3385G>C | NP_000483.3:p.Val1129Leu | |
| XM_011515751.1:c.3475G>C | XP_011514053.1:p.Val1159Leu | |
| XM_011515752.1:c.3475G>C | XP_011514054.1:p.Val1159Leu | |
| XM_011515753.1:c.3142G>C | XP_011514055.1:p.Val1048Leu | |
| XM_011515754.1:c.3142G>C | XP_011514056.1:p.Val1048Leu | |
| NM_000492.4:c.3385G>C MANE Select | NP_000483.3:p.Val1129Leu |