Linked Data
ClinVar Variation Id:
143969
dbSNP Id:
rs587776420
ExAC:
16:23634397 AG / A
gnomAD v2:
16-23634397-AG-A
gnomAD v3:
16-23623076-AG-A
gnomAD v4:
16-23623076-AG-A
PubMed:
PMID:25099575
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23623077del , CM000678.2:g.23623077del | GRCh38 |
| NC_000016.9:g.23634398del , CM000678.1:g.23634398del | GRCh37 |
| NC_000016.8:g.23541899del | NCBI36 |
| NG_007406.1:g.23281del , LRG_308:g.23281del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000561514.3:c.2894del | ENSP00000460666.3:p.Ser965LeufsTer4 | |
| ENST00000565038.2:c.*369del | ENSP00000459882.2:n.*369del | |
| ENST00000566069.6:c.2888del | ENSP00000459237.2:p.Ser963LeufsTer4 | |
| ENST00000697377.2:c.2732del | ENSP00000513286.2:p.Ser911LeufsTer4 | |
| ENST00000697379.2:c.2894del | ENSP00000513287.2:p.Ser965LeufsTer4 | |
| ENST00000561514.2:c.2003del | ENSP00000460666.2:p.Ser668LeufsTer4 | |
| ENST00000697374.1:c.2003del | ENSP00000513284.1:p.Ser668LeufsTer4 | |
| ENST00000697375.1:n.4235del | ||
| ENST00000697376.1:c.2003del | ENSP00000513285.1:p.Ser668LeufsTer4 | |
| ENST00000697377.1:c.1841del | ENSP00000513286.1:p.Ser614LeufsTer4 | |
| ENST00000697378.1:n.3408del | ||
| ENST00000697379.1:c.2003del | ENSP00000513287.1:p.Ser668LeufsTer4 | |
| ENST00000697380.1:n.2180del | ||
| ENST00000697381.1:n.1583del | ||
| ENST00000697382.1:c.2003del | ENSP00000513288.1:p.Ser668LeufsTer4 | |
| ENST00000697383.1:c.422del | ENSP00000513289.1:p.Ser141LeufsTer4 | |
| ENST00000261584.9:c.2888del MANE Select | ENSP00000261584.4:p.Ser963LeufsTer4 | |
| ENST00000261584.8:c.2888del | ENSP00000261584.4:p.Ser963LeufsTer4 | |
| ENST00000568219.5:c.2003del | ENSP00000454703.2:p.Ser668LeufsTer4 | |
| NM_024675.3:c.2888del , LRG_308t1:c.2888del | NP_078951.2:p.Ser963LeufsTer4 | |
| XM_011545946.1:c.2894del | XP_011544248.1:p.Ser965LeufsTer4 | |
| XM_011545947.1:c.2894del | XP_011544249.1:p.Ser965LeufsTer4 | |
| XM_011545948.1:c.2003del | XP_011544250.1:p.Ser668LeufsTer4 | |
| XR_950851.1:n.3684del | ||
| XM_011545946.2:c.2894del | XP_011544248.1:p.Ser965LeufsTer4 | |
| XM_011545947.2:c.2894del | XP_011544249.1:p.Ser965LeufsTer4 | |
| XM_011545948.2:c.2003del | XP_011544250.1:p.Ser668LeufsTer4 | |
| XM_017023671.1:c.2894del | XP_016879160.1:p.Ser965LeufsTer4 | |
| XM_017023672.2:c.2888del | XP_016879161.1:p.Ser963LeufsTer4 | |
| XM_017023673.2:c.2888del | XP_016879162.1:p.Ser963LeufsTer4 | |
| NM_024675.4:c.2888del MANE Select | NP_078951.2:p.Ser963LeufsTer4 |