WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Linked Data
ClinVar Variation Id:
16914
ClinVar RCV Id:
RCV000018414
dbSNP Id:
rs786205878
MyVariant Identifiers:
chr7:g.75610417_75610429dupTACGTGGACAAGC (hg19)
chr7:g.75981099_75981111dupTACGTGGACAAGC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.75981099_75981111dup , CM000669.2:g.75981099_75981111dup | GRCh38 |
| NC_000007.13:g.75610417_75610429dup , CM000669.1:g.75610417_75610429dup | GRCh37 |
| NC_000007.12:g.75448353_75448365dup | NCBI36 |
| NG_008930.1:g.70998_71010dup |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000475509.2:c.343_355dup | ENSP00000516446.1:p.Arg119LeufsTer16 | |
| ENST00000706544.1:c.568_580dup | ENSP00000516442.1:p.Arg194LeufsTer16 | |
| ENST00000706545.1:c.568_580dup | ENSP00000516443.1:p.Arg194LeufsTer16 | |
| ENST00000706546.1:c.568_580dup | ENSP00000516444.1:p.Arg194LeufsTer16 | |
| ENST00000706547.1:c.568_580dup | ENSP00000516445.1:p.Arg194LeufsTer16 | |
| ENST00000461988.6:c.568_580dup MANE Select | ENSP00000419970.1:p.Arg194LeufsTer16 | |
| ENST00000394893.5:c.568_580dup | ENSP00000378355.1:p.Arg194LeufsTer16 | |
| ENST00000412064.6:c.566+2_566+14dup | ENSP00000404731.2:n.566+2_566+14dup | |
| ENST00000447222.5:c.719_731dup | ||
| ENST00000454934.5:c.517-418_517-406dup | ENSP00000414263.1:n.517-418_517-406dup | |
| ENST00000460892.1:n.168_180dup | ||
| ENST00000461988.5:c.568_580dup | ENSP00000419970.1:p.Arg194LeufsTer16 | |
| NM_000941.2:c.568_580dup | NP_000932.3:p.Arg194LeufsTer16 | |
| NM_000941.3:c.568_580dup | NP_000932.3:p.Arg194LeufsTer16 | |
| NM_001367562.1:c.568_580dup | NP_001354491.1:p.Arg194LeufsTer16 | |
| NM_001382655.1:c.622_634dup | NP_001369584.1:p.Arg212LeufsTer16 | |
| NM_001382657.1:c.568_580dup | NP_001369586.1:p.Arg194LeufsTer16 | |
| NM_001382658.1:c.568_580dup | NP_001369587.1:p.Arg194LeufsTer16 | |
| NM_001382659.1:c.568_580dup | NP_001369588.1:p.Arg194LeufsTer16 | |
| NM_001382662.1:c.568_580dup | NP_001369591.1:p.Arg194LeufsTer16 | |
| NM_001367562.3:c.559_571dup | NP_001354491.2:p.Arg191LeufsTer16 | |
| NM_001382655.3:c.613_625dup | NP_001369584.2:p.Arg209LeufsTer16 | |
| NM_001382657.2:c.559_571dup | NP_001369586.2:p.Arg191LeufsTer16 | |
| NM_001382658.3:c.559_571dup | NP_001369587.2:p.Arg191LeufsTer16 | |
| NM_001382659.3:c.559_571dup | NP_001369588.2:p.Arg191LeufsTer16 | |
| NM_001382662.3:c.559_571dup | NP_001369591.2:p.Arg191LeufsTer16 | |
| NM_001395413.1:c.559_571dup MANE Select | NP_001382342.1:p.Arg191LeufsTer16 |