Linked Data
ClinVar Variation Id:
934263
ClinVar RCV Id:
RCV001202618
dbSNP Id:
rs2046948026
MyVariant Identifiers:
chr17:g.17120383C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.17217069C>G , CM000679.2:g.17217069C>G | GRCh38 |
| NC_000017.10:g.17120383C>G , CM000679.1:g.17120383C>G | GRCh37 |
| NC_000017.9:g.17061108C>G | NCBI36 |
| NG_008001.2:g.25120G>C , LRG_325:g.25120G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000285071.9:c.1176G>C (FLCN) MANE Select | ENSP00000285071.4:p.Arg392= | |
| ENST00000285071.8:c.1176G>C (FLCN) | ENSP00000285071.4:p.Arg392= | |
| ENST00000427497.3:c.*10G>C | ENSP00000394249.3:n.*10G>C | |
| ENST00000577591.1:n.199G>C (FLCN) | ||
| ENST00000578209.5:c.562-421C>G (MPRIP) | ||
| NM_144997.5:c.1176G>C , LRG_325t1:c.1176G>C (FLCN) | NP_659434.2:p.Arg392= | |
| XM_011523714.1:c.1230G>C (FLCN) | XP_011522016.1:p.Arg410= | |
| XM_011523715.1:c.1230G>C (FLCN) | XP_011522017.1:p.Arg410= | |
| XM_011523716.1:c.1230G>C (FLCN) | XP_011522018.1:p.Arg410= | |
| XM_011523717.1:c.1230G>C (FLCN) | XP_011522019.1:p.Arg410= | |
| XM_011523718.1:c.1230G>C (FLCN) | XP_011522020.1:p.Arg410= | |
| XM_011523719.1:c.1230G>C (FLCN) | XP_011522021.1:p.Arg410= | |
| XM_011523720.1:c.954G>C (FLCN) | XP_011522022.1:p.Arg318= | |
| XM_011523721.1:c.1230G>C (FLCN) | XP_011522023.1:p.Arg410= | |
| XR_934007.1:n.2570G>C (FLCN) | ||
| NM_001353229.1:c.1230G>C (FLCN) | NP_001340158.1:p.Arg410= | |
| NM_001353230.1:c.1176G>C (FLCN) | NP_001340159.1:p.Arg392= | |
| NM_001353231.1:c.1176G>C (FLCN) | NP_001340160.1:p.Arg392= | |
| NM_144997.6:c.1176G>C (FLCN) | NP_659434.2:p.Arg392= | |
| XM_011523714.3:c.1230G>C (FLCN) | XP_011522016.1:p.Arg410= | |
| XM_011523718.3:c.1230G>C (FLCN) | XP_011522020.1:p.Arg410= | |
| XM_011523719.3:c.1230G>C (FLCN) | XP_011522021.1:p.Arg410= | |
| XM_011523721.3:c.1230G>C (FLCN) | XP_011522023.1:p.Arg410= | |
| XM_017024305.2:c.1230G>C (FLCN) | XP_016879794.1:p.Arg410= | |
| XM_017024308.1:c.1176G>C (FLCN) | XP_016879797.1:p.Arg392= | |
| XM_017024309.2:c.954G>C (FLCN) | XP_016879798.1:p.Arg318= | |
| XM_024450635.1:c.1230G>C (FLCN) | XP_024306403.1:p.Arg410= | |
| XR_001752445.2:n.1734G>C (FLCN) | ||
| NM_144997.7:c.1176G>C (FLCN) MANE Select | NP_659434.2:p.Arg392= | |
| NM_001353229.2:c.1230G>C (FLCN) | NP_001340158.1:p.Arg410= | |
| NM_001353230.2:c.1176G>C (FLCN) | NP_001340159.1:p.Arg392= | |
| NM_001353231.2:c.1176G>C (FLCN) | NP_001340160.1:p.Arg392= |