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
dbSNP Id:
rs773225914
ExAC:
16:2327910 ACTC / A
gnomAD v2:
16-2327910-ACTC-A
gnomAD v3:
16-2277909-ACTC-A
gnomAD v4:
16-2277909-ACTC-A
MyVariant Identifiers:
chr16:g.2327911_2327913del (hg19)
chr16:g.2277911_2277913del (hg38)
chr16:g.2277910_2277912del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2277914_2277916del , CM000678.2:g.2277914_2277916del | GRCh38 |
| NC_000016.9:g.2327915_2327917del , CM000678.1:g.2327915_2327917del | GRCh37 |
| NC_000016.8:g.2267916_2267918del | NCBI36 |
| NG_011790.1:g.67835_67837del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301732.10:c.4876_4878del MANE Select | ENSP00000301732.5:p.Glu1626del | |
| ENST00000301732.9:c.4876_4878del | ENSP00000301732.5:p.Glu1626del | |
| ENST00000382381.7:c.4702_4704del | ENSP00000371818.3:p.Glu1568del | |
| NM_001089.2:c.4876_4878del | NP_001080.2:p.Glu1626del | |
| NM_001089.3:c.4876_4878del MANE Select | NP_001080.2:p.Glu1626del |