Linked Data
ClinVar Variation Id:
1052521
ClinVar RCV Id:
RCV001360720
dbSNP Id:
rs1924590267
COSMIC:
COSM4469217
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.85878985G>A , CM000685.2:g.85878985G>A | GRCh38 |
| NC_000023.10:g.85133990G>A , CM000685.1:g.85133990G>A | GRCh37 |
| NC_000023.9:g.85020646G>A | NCBI36 |
| NG_009874.2:g.173578C>T , LRG_699:g.173578C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357749.7:c.1589C>T MANE Select | ENSP00000350386.2:p.Pro530Leu | |
| ENST00000357749.6:c.1589C>T | ENSP00000350386.2:p.Pro530Leu | |
| ENST00000467744.2:n.127-15891C>T | ||
| NM_000390.2:c.1589C>T , LRG_699t1:c.1589C>T | NP_000381.1:p.Pro530Leu | |
| XM_006724615.2:c.1526C>T | XP_006724678.1:p.Pro509Leu | |
| XM_011530839.1:c.1145C>T | XP_011529141.1:p.Pro382Leu | |
| NM_000390.3:c.1589C>T | NP_000381.1:p.Pro530Leu | |
| NM_001320959.1:c.1145C>T | NP_001307888.1:p.Pro382Leu | |
| NM_001362517.1:c.1145C>T | NP_001349446.1:p.Pro382Leu | |
| NM_001362518.1:c.1145C>T | NP_001349447.1:p.Pro382Leu | |
| NM_001362519.1:c.1145C>T | NP_001349448.1:p.Pro382Leu | |
| XM_017029242.2:c.1589C>T | XP_016884731.1:p.Pro530Leu | |
| XM_017029246.1:c.1145C>T | XP_016884735.1:p.Pro382Leu | |
| XM_024452331.1:c.1145C>T | XP_024308099.1:p.Pro382Leu | |
| NM_000390.4:c.1589C>T MANE Select | NP_000381.1:p.Pro530Leu | |
| NM_001362518.2:c.1145C>T | NP_001349447.1:p.Pro382Leu |