Linked Data
ClinVar Variation Id:
51962
ClinVar RCV Id:
RCV000257211
dbSNP Id:
rs397507811
PubMed:
PMID:12655567
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.32340253del , CM000675.2:g.32340253del | GRCh38 |
| NC_000013.10:g.32914390del , CM000675.1:g.32914390del | GRCh37 |
| NC_000013.9:g.31812390del | NCBI36 |
| NG_012772.3:g.29774del , LRG_293:g.29774del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000470094.2:c.5898del | ENSP00000434898.2:p.His1966GlnfsTer? | |
| ENST00000528762.2:c.5898del | ENSP00000433168.2:p.His1966GlnfsTer? | |
| ENST00000530893.7:c.5529del | ENSP00000499438.2:p.His1843GlnfsTer? | |
| ENST00000665585.2:c.5898del | ENSP00000499570.2:p.His1966GlnfsTer? | |
| ENST00000666593.2:c.5898del | ENSP00000499256.2:p.His1966GlnfsTer? | |
| ENST00000700202.2:c.5898del | ENSP00000514856.2:p.His1966GlnfsTer? | |
| ENST00000380152.8:c.5898del MANE Select | ENSP00000369497.3:p.His1966GlnfsTer? | |
| ENST00000544455.6:c.5898del | ENSP00000439902.1:p.His1966GlnfsTer? | |
| ENST00000614259.2:c.5898del | ENSP00000506251.1:p.His1966GlnfsTer? | |
| ENST00000680887.1:c.5898del | ENSP00000505508.1:p.His1966GlnfsTer? | |
| ENST00000380152.7:c.5898del | ENSP00000369497.3:p.His1966GlnfsTer? | |
| ENST00000544455.5:c.5898del | ENSP00000439902.1:p.His1966GlnfsTer? | |
| ENST00000614259.1:n.5898del | ||
| NM_000059.3:c.5898del , LRG_293t1:c.5898del | NP_000050.2:p.His1966GlnfsTer? | |
| XM_011535203.1:c.5898del | XP_011533505.1:p.His1966GlnfsTer? | |
| XM_011535204.1:c.5898del | XP_011533506.1:p.His1966GlnfsTer? | |
| XM_011535205.1:c.5898del | XP_011533507.1:p.His1966GlnfsTer? | |
| NM_000059.4:c.5898del MANE Select | NP_000050.3:p.His1966GlnfsTer? |