Linked Data
ClinVar Variation Id:
942015
ClinVar RCV Id:
RCV001211916
dbSNP Id:
rs2032704685
COSMIC:
COSM5415298
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.142513626G>T , CM000665.2:g.142513626G>T | GRCh38 |
| NC_000003.11:g.142232468G>T , CM000665.1:g.142232468G>T | GRCh37 |
| NC_000003.10:g.143715158G>T | NCBI36 |
| NG_008951.1:g.70201C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000350721.9:c.4516C>A MANE Select | ENSP00000343741.4:p.Leu1506Ile | |
| ENST00000653868.1:n.4545C>A | ||
| ENST00000656590.1:c.3306C>A | ||
| ENST00000661310.1:c.4324C>A | ENSP00000499589.1:p.Leu1442Ile | |
| ENST00000350721.8:c.4516C>A | ENSP00000343741.4:p.Leu1506Ile | |
| NM_001184.3:c.4516C>A | NP_001175.2:p.Leu1506Ile | |
| XM_011512924.1:c.4522C>A | XP_011511226.1:p.Leu1508Ile | |
| XM_011512925.1:c.4330C>A | XP_011511227.1:p.Leu1444Ile | |
| XM_011512926.1:c.4522C>A | XP_011511228.1:p.Leu1508Ile | |
| XM_011512927.1:c.4522C>A | XP_011511229.1:p.Leu1508Ile | |
| XR_924147.1:n.4611C>A | ||
| XR_924148.1:n.4611C>A | ||
| XR_924149.1:n.4611C>A | ||
| NM_001354579.1:c.4324C>A | NP_001341508.1:p.Leu1442Ile | |
| XR_001740179.2:n.4605C>A | ||
| XR_001740180.2:n.4611C>A | ||
| XR_001740181.2:n.4611C>A | ||
| XR_001740182.1:n.4611C>A | ||
| XR_002959543.1:n.4611C>A | ||
| XR_924148.2:n.4611C>A | ||
| NM_001184.4:c.4516C>A MANE Select | NP_001175.2:p.Leu1506Ile | |
| NM_001354579.2:c.4324C>A | NP_001341508.1:p.Leu1442Ile |