Linked Data
ClinVar Variation Id:
552149
dbSNP Id:
rs1554389346
MyVariant Identifiers:
chr7:g.117592211del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.117592211del , CM000669.2:g.117592211del | GRCh38 |
| NC_000007.13:g.117232265del , CM000669.1:g.117232265del | GRCh37 |
| NC_000007.12:g.117019501del | NCBI36 |
| NG_016465.4:g.131428del , LRG_663:g.131428del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647720.2:c.2044del | ENSP00000497673.2:p.Thr682GlnfsTer? | |
| ENST00000647978.2:c.*1758del | ENSP00000497658.1:n.*1758del | |
| ENST00000649781.2:c.1861del | ENSP00000497203.1:p.Thr621GlnfsTer? | |
| ENST00000685018.2:c.2044del | ENSP00000510194.2:p.Thr682GlnfsTer? | |
| ENST00000687278.2:c.2044del | ENSP00000509593.2:p.Thr682GlnfsTer? | |
| ENST00000699585.1:c.2044del | ENSP00000514456.1:p.Thr682GlnfsTer? | |
| ENST00000699598.1:c.2044del | ENSP00000514467.1:p.Thr682GlnfsTer? | |
| ENST00000699599.1:c.2044del | ENSP00000514468.1:p.Thr682GlnfsTer? | |
| ENST00000699600.1:c.2044del | ENSP00000514469.1:p.Thr682GlnfsTer? | |
| ENST00000699601.1:c.*344del | ENSP00000514470.1:n.*344del | |
| ENST00000699602.1:c.2044del | ENSP00000514471.1:p.Thr682GlnfsTer? | |
| ENST00000699604.1:c.*1868del | ENSP00000514472.1:n.*1868del | |
| ENST00000699605.1:c.1618del | ENSP00000514473.1:p.Thr540GlnfsTer? | |
| ENST00000003084.11:c.2044del MANE Select | ENSP00000003084.6:p.Thr682GlnfsTer? | |
| ENST00000647978.1:c.*1758del | ENSP00000497658.1:n.*1758del | |
| ENST00000648260.1:c.1402-10615del | ENSP00000497957.1:n.1402-10615del | |
| ENST00000649406.1:c.1861del | ENSP00000497965.1:p.Thr621GlnfsTer? | |
| ENST00000649781.1:c.1861del | ENSP00000497203.1:p.Thr621GlnfsTer? | |
| ENST00000003084.10:c.2044del | ENSP00000003084.6:p.Thr682GlnfsTer? | |
| ENST00000426809.5:c.1954del | ENSP00000389119.1:p.Thr652GlnfsTer? | |
| NM_000492.3:c.2044del , LRG_663t1:c.2044del | NP_000483.3:p.Thr682GlnfsTer? | |
| XM_011515751.1:c.2134del | XP_011514053.1:p.Thr712GlnfsTer? | |
| XM_011515752.1:c.2134del | XP_011514054.1:p.Thr712GlnfsTer? | |
| XM_011515753.1:c.1801del | XP_011514055.1:p.Thr601GlnfsTer? | |
| XM_011515754.1:c.1801del | XP_011514056.1:p.Thr601GlnfsTer? | |
| NM_000492.4:c.2044del MANE Select | NP_000483.3:p.Thr682GlnfsTer? |