Linked Data
ClinVar Variation Id:
1365985
ClinVar RCV Id:
RCV001930005
dbSNP Id:
rs1891718902
MyVariant Identifiers:
chr15:g.35084387G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34792186G>A , CM000677.2:g.34792186G>A | GRCh38 |
| NC_000015.9:g.35084387G>A , CM000677.1:g.35084387G>A | GRCh37 |
| NC_000015.8:g.32871679G>A | NCBI36 |
| NG_007553.1:g.8541C>T , LRG_388:g.8541C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.818C>T (ACTC1) | ||
| ENST00000290378.6:c.712C>T (ACTC1) MANE Select | ENSP00000290378.4:p.Leu238= | |
| ENST00000647798.1:n.806C>T (ACTC1) | ||
| ENST00000650163.1:n.792C>T (ACTC1) | ||
| ENST00000290378.4:c.712C>T (ACTC1) | ENSP00000290378.4:p.Leu238= | |
| ENST00000557860.1:n.402C>T (ACTC1) | ||
| ENST00000560563.1:n.211C>T (ACTC1) | ||
| NM_005159.4:c.712C>T , LRG_388t1:c.712C>T (ACTC1) | NP_005150.1:p.Leu238= | |
| NR_120329.1:n.299+14755G>A (GJD2-DT) | ||
| NM_005159.5:c.712C>T (ACTC1) MANE Select | NP_005150.1:p.Leu238= |