Linked Data
ClinVar Variation Id:
854942
ClinVar RCV Id:
RCV001060093
dbSNP Id:
rs1312745277
COSMIC:
COSM5967361
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.67686100G>A , CM000685.2:g.67686100G>A | GRCh38 |
| NC_000023.10:g.66905942G>A , CM000685.1:g.66905942G>A | GRCh37 |
| NC_000023.9:g.66822667G>A | NCBI36 |
| NG_009014.2:g.147069G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396043.4:c.*207G>A | ENSP00000379358.4:n.*207G>A | |
| ENST00000374690.9:c.1859G>A MANE Select | ENSP00000363822.3:p.Cys620Tyr | |
| ENST00000396043.3:c.486G>A | ENSP00000379358.3:n.486G>A | |
| ENST00000396044.8:c.1859G>A | ENSP00000379359.3:p.Cys620Tyr | |
| ENST00000612452.5:c.1859G>A | ENSP00000484033.2:p.Cys620Tyr | |
| ENST00000374690.7:c.1859G>A | ENSP00000363822.3:p.Cys620Tyr | |
| ENST00000396043.2:c.263G>A | ENSP00000379358.2:p.Cys88Tyr | |
| ENST00000396044.7:c.1859G>A | ENSP00000379359.3:p.Cys620Tyr | |
| ENST00000504326.5:c.1859G>A | ENSP00000421155.1:p.Cys620Tyr | |
| ENST00000513847.5:n.2186G>A | ||
| ENST00000514029.5:c.*340G>A | ENSP00000425199.1:n.*340G>A | |
| ENST00000612010.4:c.*211G>A | ENSP00000482407.1:n.*211G>A | |
| ENST00000612452.4:c.1289G>A | ENSP00000484033.1:p.Cys430Tyr | |
| ENST00000613054.2:c.*57G>A | ENSP00000479013.1:n.*57G>A | |
| NM_000044.3:c.1859G>A | NP_000035.2:p.Cys620Tyr | |
| NM_001011645.2:c.263G>A | NP_001011645.1:p.Cys88Tyr | |
| NM_000044.4:c.1859G>A | NP_000035.2:p.Cys620Tyr | |
| NM_001011645.3:c.263G>A | NP_001011645.1:p.Cys88Tyr | |
| NM_001348061.1:c.1859G>A | NP_001334990.1:p.Cys620Tyr | |
| NM_001348063.1:c.1859G>A | NP_001334992.1:p.Cys620Tyr | |
| NM_001348064.1:c.*57G>A | NP_001334993.1:n.*57G>A | |
| NM_000044.6:c.1859G>A MANE Select | NP_000035.2:p.Cys620Tyr |