Linked Data
ClinVar Variation Id:
10027
dbSNP Id:
rs111033618
gnomAD v4:
X-71109321-G-A
ERepo:
CA120885/MONDO:0010315/129
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.71109321G>A , CM000685.2:g.71109321G>A | GRCh38 |
| NC_000023.10:g.70329171G>A , CM000685.1:g.70329171G>A | GRCh37 |
| NC_000023.9:g.70245896G>A | NCBI36 |
| NG_009088.1:g.7233C>T , LRG_150:g.7233C>T | |
| NG_021141.1:g.2468C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000482750.6:c.664C>T | ENSP00000421262.2:p.Arg222Cys | |
| ENST00000696903.1:n.715C>T | ||
| ENST00000374202.7:c.664C>T MANE Select | ENSP00000363318.3:p.Arg222Cys | |
| ENST00000642473.1:n.1028C>T | ||
| ENST00000644022.1:n.930C>T | ||
| ENST00000644708.1:n.1070C>T | ||
| ENST00000644911.1:n.1070C>T | ||
| ENST00000645266.1:c.664C>T | ENSP00000493734.1:p.Arg222Cys | |
| ENST00000645518.1:c.664C>T | ENSP00000493986.1:p.Arg222Cys | |
| ENST00000646106.1:c.664C>T | ENSP00000496437.1:p.Arg222Cys | |
| ENST00000646505.1:c.664C>T | ENSP00000496673.1:p.Arg222Cys | |
| ENST00000647492.1:c.664C>T | ENSP00000495340.1:p.Arg222Cys | |
| ENST00000276110.6:n.1257C>T | ||
| ENST00000374188.7:c.-53C>T | ENSP00000363303.3:n.-53C>T | |
| ENST00000374202.6:c.664C>T | ENSP00000363318.2:p.Arg222Cys | |
| ENST00000456850.6:c.94C>T | ENSP00000388967.2:p.Arg32Cys | |
| ENST00000464642.5:c.532C>T | ENSP00000425233.1:p.Arg178Cys | |
| ENST00000482750.5:c.77C>T | ||
| ENST00000512747.3:n.591C>T | ||
| NM_000206.2:c.664C>T , LRG_150t1:c.664C>T | NP_000197.1:p.Arg222Cys | |
| NM_000206.3:c.664C>T MANE Select | NP_000197.1:p.Arg222Cys |