Linked Data
ClinVar Variation Id:
55431
ClinVar RCV Id:
RCV002496718
dbSNP Id:
rs273901746
gnomAD v4:
17-43063374-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43063375del , CM000679.2:g.43063375del | GRCh38 |
| NC_000017.10:g.41215392del , CM000679.1:g.41215392del | GRCh37 |
| NC_000017.9:g.38468918del | NCBI36 |
| NG_005905.2:g.154609del , LRG_292:g.154609del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000461574.2:c.5150-2del | ENSP00000417241.2:n.5150-2del | |
| ENST00000470026.6:c.5153-2del | ENSP00000419274.2:n.5153-2del | |
| ENST00000473961.6:c.5027-2del | ENSP00000420201.2:n.5027-2del | |
| ENST00000476777.6:c.5147-2del | ENSP00000417554.2:n.5147-2del | |
| ENST00000477152.6:c.5075-2del | ENSP00000419988.2:n.5075-2del | |
| ENST00000478531.6:c.1841-2del | ENSP00000420412.2:n.1841-2del | |
| ENST00000489037.2:c.5075-2del | ENSP00000420781.2:n.5075-2del | |
| ENST00000493919.6:c.1703-2del | ENSP00000418819.2:n.1703-2del | |
| ENST00000494123.6:c.5153-2del | ENSP00000419103.2:n.5153-2del | |
| ENST00000497488.2:c.4265-2del | ENSP00000418986.2:n.4265-2del | |
| ENST00000618469.2:c.5153-2del | ENSP00000478114.2:n.5153-2del | |
| ENST00000634433.2:c.5030-2del | ENSP00000489431.2:n.5030-2del | |
| ENST00000644379.2:c.5219-2del | ENSP00000496570.2:n.5219-2del | |
| ENST00000644555.2:c.1703-2del | ENSP00000494614.2:n.1703-2del | |
| ENST00000652672.2:c.5012-2del | ENSP00000498906.2:n.5012-2del | |
| ENST00000484087.6:c.1715-2del | ENSP00000419481.2:n.1715-2del | |
| ENST00000357654.9:c.5153-2del MANE Select | ENSP00000350283.3:n.5153-2del | |
| ENST00000471181.7:c.5216-2del | ENSP00000418960.2:n.5216-2del | |
| ENST00000644379.1:c.1540-2del | ||
| ENST00000352993.7:c.1727-2del | ENSP00000312236.5:n.1727-2del | |
| ENST00000357654.7:c.5153-2del | ENSP00000350283.3:n.5153-2del | |
| ENST00000461221.5:c.*4936-2del | ENSP00000418548.1:n.*4936-2del | |
| ENST00000468300.5:c.1841-2del | ENSP00000417148.1:n.1841-2del | |
| ENST00000471181.6:c.5216-2del | ENSP00000418960.2:n.5216-2del | |
| ENST00000478531.5:c.1841-2del | ENSP00000420412.1:n.1841-2del | |
| ENST00000484087.5:c.1466-2del | ENSP00000419481.1:n.1466-2del | |
| ENST00000491747.6:c.1841-2del | ENSP00000420705.2:n.1841-2del | |
| ENST00000493795.5:c.5012-2del | ENSP00000418775.1:n.5012-2del | |
| ENST00000493919.5:c.1703-2del | ENSP00000418819.1:n.1703-2del | |
| ENST00000586385.5:c.83-2del | ENSP00000465818.1:n.83-2del | |
| ENST00000591534.5:c.626-2del | ENSP00000467329.1:n.626-2del | |
| ENST00000591849.5:c.-98-13185del | ENSP00000465347.1:n.-98-13185del | |
| NM_007294.3:c.5153-2del , LRG_292t1:c.5153-2del | NP_009225.1:n.5153-2del | |
| NM_007297.3:c.5012-2del | NP_009228.2:n.5012-2del | |
| NM_007298.3:c.1841-2del | NP_009229.2:n.1841-2del | |
| NM_007299.3:c.1841-2del | NP_009230.2:n.1841-2del | |
| NM_007300.3:c.5216-2del | NP_009231.2:n.5216-2del | |
| NR_027676.1:n.5289-2del | ||
| NM_007294.4:c.5153-2del MANE Select | NP_009225.1:n.5153-2del | |
| NM_007297.4:c.5012-2del | NP_009228.2:n.5012-2del | |
| NM_007299.4:c.1841-2del | NP_009230.2:n.1841-2del | |
| NM_007300.4:c.5216-2del | NP_009231.2:n.5216-2del | |
| NR_027676.2:n.5330-2del |