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:
128121
dbSNP Id:
rs587780206
MyVariant Identifiers:
chr16:g.23646191_23646192delinsCA (hg19)
chr16:g.23634870_23634871delinsCA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.23634870_23634871delinsCA , CM000678.2:g.23634870_23634871delinsCA | GRCh38 |
| NC_000016.9:g.23646191_23646192delinsCA , CM000678.1:g.23646191_23646192delinsCA | GRCh37 |
| NC_000016.8:g.23553692_23553693delinsCA | NCBI36 |
| NG_007406.1:g.11487_11488delinsTG , LRG_308:g.11487_11488delinsTG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000561514.3:c.1681_1682delinsTG | ENSP00000460666.3:p.Gln561Ter | |
| ENST00000565038.2:c.211+2979_211+2980delinsTG | ENSP00000459882.2:n.211+2979_211+2980deli... | |
| ENST00000566069.6:c.1675_1676delinsTG | ENSP00000459237.2:p.Gln559Ter | |
| ENST00000697377.2:c.1681_1682delinsTG | ENSP00000513286.2:p.Gln561Ter | |
| ENST00000697379.2:c.1681_1682delinsTG | ENSP00000513287.2:p.Gln561Ter | |
| ENST00000561514.2:c.790_791delinsTG | ENSP00000460666.2:p.Gln264Ter | |
| ENST00000697374.1:c.790_791delinsTG | ENSP00000513284.1:p.Gln264Ter | |
| ENST00000697375.1:n.3022_3023delinsTG | ||
| ENST00000697376.1:c.790_791delinsTG | ENSP00000513285.1:p.Gln264Ter | |
| ENST00000697377.1:c.790_791delinsTG | ENSP00000513286.1:p.Gln264Ter | |
| ENST00000697378.1:n.2195_2196delinsTG | ||
| ENST00000697379.1:c.790_791delinsTG | ENSP00000513287.1:p.Gln264Ter | |
| ENST00000697382.1:c.790_791delinsTG | ENSP00000513288.1:p.Gln264Ter | |
| ENST00000697383.1:c.49-5596_49-5595delinsTG | ENSP00000513289.1:n.49-5596_49-5595delins... | |
| ENST00000697384.1:n.1829_1830delinsTG | ||
| ENST00000261584.9:c.1675_1676delinsTG MANE Select | ENSP00000261584.4:p.Gln559Ter | |
| ENST00000261584.8:c.1675_1676delinsTG | ENSP00000261584.4:p.Gln559Ter | |
| ENST00000565038.1:c.86+2979_86+2980delinsTG | ||
| ENST00000568219.5:c.790_791delinsTG | ENSP00000454703.2:p.Gln264Ter | |
| NM_024675.3:c.1675_1676delinsTG , LRG_308t1:c.1675_1676delinsTG | NP_078951.2:p.Gln559Ter | |
| XM_011545946.1:c.1681_1682delinsTG | XP_011544248.1:p.Gln561Ter | |
| XM_011545947.1:c.1681_1682delinsTG | XP_011544249.1:p.Gln561Ter | |
| XM_011545948.1:c.790_791delinsTG | XP_011544250.1:p.Gln264Ter | |
| XR_950851.1:n.2471_2472delinsTG | ||
| XM_011545946.2:c.1681_1682delinsTG | XP_011544248.1:p.Gln561Ter | |
| XM_011545947.2:c.1681_1682delinsTG | XP_011544249.1:p.Gln561Ter | |
| XM_011545948.2:c.790_791delinsTG | XP_011544250.1:p.Gln264Ter | |
| XM_017023671.1:c.1681_1682delinsTG | XP_016879160.1:p.Gln561Ter | |
| XM_017023672.2:c.1675_1676delinsTG | XP_016879161.1:p.Gln559Ter | |
| XM_017023673.2:c.1675_1676delinsTG | XP_016879162.1:p.Gln559Ter | |
| NM_024675.4:c.1675_1676delinsTG MANE Select | NP_078951.2:p.Gln559Ter |