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
gnomAD v4:
6-31354908-C-CCAG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31354910_31354911insGCA , CM000668.2:g.31354910_31354911insGCA | GRCh38 |
| NC_000006.11:g.31322687_31322688insGCA , CM000668.1:g.31322687_31322688insGCA | GRCh37 |
| NC_000006.10:g.31430666_31430667insGCA | NCBI36 |
| NG_023187.1:g.7304_7305insCTG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000474381.2:n.3059+198_3059+199insCTG | ||
| ENST00000481849.6:n.2776_2777insCTG | ||
| ENST00000497377.6:n.2683_2684insCTG | ||
| ENST00000640094.2:c.896-244_896-243insCTG | ENSP00000491275.2:n.896-244_896-243insCTG... | |
| ENST00000696558.1:c.1081+198_1081+199insCTG | ENSP00000512716.1:n.1081+198_1081+199insC... | |
| ENST00000696559.1:c.1012+198_1012+199insCTG | ENSP00000512717.1:n.1012+198_1012+199insC... | |
| ENST00000696560.1:c.1012+198_1012+199insCTG | ENSP00000512718.1:n.1012+198_1012+199insC... | |
| ENST00000696561.1:c.1012+198_1012+199insCTG | ENSP00000512719.1:n.1012+198_1012+199insC... | |
| ENST00000696562.1:c.1012+198_1012+199insCTG | ENSP00000512720.1:n.1012+198_1012+199insC... | |
| ENST00000412585.7:c.1012+198_1012+199insCTG MANE Select | ENSP00000399168.2:n.1012+198_1012+199insC... | |
| ENST00000640094.1:c.89-244_89-243insCTG | ENSP00000491275.1:n.89-244_89-243insCTG | |
| ENST00000412585.6:c.1012+198_1012+199insCTG | ENSP00000399168.2:n.1012+198_1012+199insC... | |
| ENST00000497377.5:n.168_169insCTG | ||
| NM_005514.6:c.1012+198_1012+199insCTG | NP_005505.2:n.1012+198_1012+199insCTG | |
| XM_011514556.1:c.1045+198_1045+199insCTG | XP_011512858.1:n.1045+198_1045+199insCTG | |
| XM_011514557.1:c.896-244_896-243insCTG | XP_011512859.1:n.896-244_896-243insCTG | |
| XR_926175.1:n.1451+198_1451+199insCTG | ||
| NM_005514.7:c.1012+198_1012+199insCTG | NP_005505.2:n.1012+198_1012+199insCTG | |
| NM_005514.8:c.1012+198_1012+199insCTG MANE Select | NP_005505.2:n.1012+198_1012+199insCTG |