Linked Data
ClinVar Variation Id:
1937194
ClinVar RCV Id:
RCV002642747
MyVariant Identifiers:
chr11:g.6415483G>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6394253G>C , CM000673.2:g.6394253G>C | GRCh38 |
| NC_000011.9:g.6415483G>C , CM000673.1:g.6415483G>C | GRCh37 |
| NC_000011.8:g.6372059G>C | NCBI36 |
| NG_011780.1:g.8829G>C | |
| NG_029615.1:g.30162C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.1542G>C MANE Select | ENSP00000340409.4:p.Leu514= | |
| ENST00000342245.8:c.1542G>C | ENSP00000340409.4:p.Leu514= | |
| ENST00000526280.1:c.599G>C | ||
| ENST00000527275.5:c.1539G>C | ENSP00000435350.1:p.Leu513= | |
| ENST00000531303.5:c.*393G>C | ENSP00000432625.1:n.*393G>C | |
| ENST00000531336.1:n.530G>C | ||
| ENST00000533123.5:c.*269G>C | ENSP00000435950.1:n.*269G>C | |
| ENST00000534405.5:c.*373G>C | ENSP00000434353.1:n.*373G>C | |
| NM_000543.4:c.1542G>C | NP_000534.3:p.Leu514= | |
| NM_001007593.2:c.1539G>C | NP_001007594.2:p.Leu513= | |
| XM_005253075.3:c.*35G>C | XP_005253132.1:n.*35G>C | |
| XM_011520303.1:c.1410G>C | XP_011518605.1:p.Leu470= | |
| XM_011520304.1:c.*35G>C | XP_011518606.1:n.*35G>C | |
| NM_001318087.1:c.*35G>C | NP_001305016.1:n.*35G>C | |
| NM_001318088.1:c.621G>C | NP_001305017.1:p.Leu207= | |
| NM_001365135.1:c.1410G>C | NP_001352064.1:p.Leu470= | |
| NR_027400.2:n.1555G>C | ||
| NR_134502.1:n.1094G>C | ||
| XM_011520304.2:c.*35G>C | XP_011518606.1:n.*35G>C | |
| XR_001747940.2:n.1727G>C | ||
| XR_002957158.1:n.1909G>C | ||
| NM_000543.5:c.1542G>C MANE Select | NP_000534.3:p.Leu514= | |
| NM_001007593.3:c.1539G>C | NP_001007594.2:p.Leu513= | |
| NM_001318087.2:c.*35G>C | NP_001305016.1:n.*35G>C | |
| NM_001318088.2:c.621G>C | NP_001305017.1:p.Leu207= | |
| NM_001365135.2:c.1410G>C | NP_001352064.1:p.Leu470= | |
| NR_027400.3:n.1495G>C | ||
| NR_134502.2:n.1034G>C |