Linked Data
ClinVar Variation Id:
7459
ClinVar RCV Id:
RCV000007885
dbSNP Id:
rs587776661
PubMed:
PMID:15617552
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.1221977del , CM000681.2:g.1221977del | GRCh38 |
| NC_000019.9:g.1221976del , CM000681.1:g.1221976del | GRCh37 |
| NC_000019.8:g.1172976del | NCBI36 |
| NG_007460.2:g.37571del , LRG_319:g.37571del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000585465.3:c.891del | ENSP00000490268.2:p.Arg297SerfsTer? | |
| ENST00000585748.3:c.519del | ENSP00000477641.2:p.Arg173SerfsTer? | |
| ENST00000585851.2:c.717del | ENSP00000467912.2:p.Arg239SerfsTer? | |
| ENST00000326873.12:c.891del MANE Select | ENSP00000324856.6:p.Arg297SerfsTer? | |
| ENST00000652231.1:c.891del | ENSP00000498804.1:p.Arg297SerfsTer? | |
| ENST00000326873.11:c.891del | ENSP00000324856.6:p.Arg297SerfsTer? | |
| ENST00000586243.5:c.891del | ENSP00000467240.2:p.Arg297SerfsTer? | |
| ENST00000589152.5:n.1589del | ||
| ENST00000591133.2:n.862del | ||
| NM_000455.4:c.891del , LRG_319t1:c.891del | NP_000446.1:p.Arg297SerfsTer? | |
| XM_005259617.1:c.891del | XP_005259674.1:p.Arg297SerfsTer? | |
| XM_005259618.3:c.891del | XP_005259675.1:p.Arg297SerfsTer? | |
| XM_011528209.1:c.669del | XP_011526511.1:p.Arg223SerfsTer? | |
| XR_936204.1:n.1667del | ||
| XM_005259617.3:c.891del | XP_005259674.1:p.Arg297SerfsTer? | |
| XM_011528209.2:c.669del | XP_011526511.1:p.Arg223SerfsTer? | |
| XR_001753738.2:n.1697del | ||
| XR_001753739.1:n.1697del | ||
| XR_001753740.2:n.1667del | ||
| NM_000455.5:c.891del MANE Select | NP_000446.1:p.Arg297SerfsTer? |