Linked Data
ClinVar Variation Id:
551113
ClinVar RCV Id:
RCV000666085
dbSNP Id:
rs1554934210
MyVariant Identifiers:
chr11:g.6391593del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.6391593del , CM000673.2:g.6391593del | GRCh38 |
| NC_000011.9:g.6412823del , CM000673.1:g.6412823del | GRCh37 |
| NC_000011.8:g.6369399del | NCBI36 |
| NG_011780.1:g.6169del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000342245.9:c.528del MANE Select | ENSP00000340409.4:p.Trp176Ter | |
| ENST00000342245.8:c.528del | ENSP00000340409.4:p.Trp176Ter | |
| ENST00000527275.5:c.525del | ENSP00000435350.1:p.Trp175Ter | |
| ENST00000530395.1:c.-95-197del | ENSP00000431479.1:n.-95-197del | |
| ENST00000531303.5:c.438+90del | ENSP00000432625.1:n.438+90del | |
| ENST00000533123.5:c.528del | ENSP00000435950.1:p.Trp176Ter | |
| ENST00000533196.1:n.375-413del | ||
| ENST00000534405.5:c.528del | ENSP00000434353.1:p.Trp176Ter | |
| NM_000543.4:c.528del | NP_000534.3:p.Trp176Ter | |
| NM_001007593.2:c.525del | NP_001007594.2:p.Trp175Ter | |
| XM_005253075.3:c.528del | XP_005253132.1:p.Trp176Ter | |
| XM_011520303.1:c.528del | XP_011518605.1:p.Trp176Ter | |
| XM_011520304.1:c.528del | XP_011518606.1:p.Trp176Ter | |
| XR_930886.1:n.826del | ||
| NM_001318087.1:c.528del | NP_001305016.1:p.Trp176Ter | |
| NM_001318088.1:c.-434del | NP_001305017.1:n.-434del | |
| NM_001365135.1:c.528del | NP_001352064.1:p.Trp176Ter | |
| NR_027400.2:n.713del | ||
| NR_134502.1:n.623+90del | ||
| XM_011520304.2:c.528del | XP_011518606.1:p.Trp176Ter | |
| XR_001747940.2:n.653del | ||
| XR_002957158.1:n.653del | ||
| NM_000543.5:c.528del MANE Select | NP_000534.3:p.Trp176Ter | |
| NM_001007593.3:c.525del | NP_001007594.2:p.Trp175Ter | |
| NM_001318087.2:c.528del | NP_001305016.1:p.Trp176Ter | |
| NM_001318088.2:c.-434del | NP_001305017.1:n.-434del | |
| NM_001365135.2:c.528del | NP_001352064.1:p.Trp176Ter | |
| NR_027400.3:n.653del | ||
| NR_134502.2:n.563+90del |