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:
376730
ClinVar RCV Id:
RCV000428356
dbSNP Id:
rs1057520031
CIViC:
CA16603138
PubMed:
PMID:16731599
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54727440A>C , CM000666.2:g.54727440A>C | GRCh38 |
| NC_000004.11:g.55593606A>C , CM000666.1:g.55593606A>C | GRCh37 |
| NC_000004.10:g.55288363A>C | NCBI36 |
| NG_007456.1:g.74446A>C , LRG_307:g.74446A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.1663A>C | ENSP00000390987.3:p.Lys555Gln | |
| ENST00000685269.1:n.1750A>C | ||
| ENST00000686011.1:c.1660A>C | ENSP00000509704.1:p.Lys554Gln | |
| ENST00000687109.1:c.1675A>C | ENSP00000509371.1:p.Lys559Gln | |
| ENST00000687208.1:n.2087A>C | ||
| ENST00000687246.1:c.1660A>C | ENSP00000509114.1:p.Lys554Gln | |
| ENST00000687265.1:n.1830A>C | ||
| ENST00000687295.1:c.1660A>C | ENSP00000509450.1:p.Lys554Gln | |
| ENST00000689832.1:c.1675A>C | ENSP00000509084.1:p.Lys559Gln | |
| ENST00000689994.1:c.1162A>C | ENSP00000509156.1:p.Lys388Gln | |
| ENST00000690543.1:c.1663A>C | ENSP00000508831.1:p.Lys555Gln | |
| ENST00000690917.1:n.1890A>C | ||
| ENST00000691361.1:n.582A>C | ||
| ENST00000692783.1:c.1672A>C | ENSP00000508733.1:p.Lys558Gln | |
| ENST00000692991.1:n.1769A>C | ||
| ENST00000288135.6:c.1672A>C MANE Select | ENSP00000288135.6:p.Lys558Gln | |
| ENST00000288135.5:c.1672A>C | ENSP00000288135.5:p.Lys558Gln | |
| ENST00000412167.6:c.1660A>C | ENSP00000390987.2:p.Lys554Gln | |
| NM_000222.2:c.1672A>C , LRG_307t1:c.1672A>C | NP_000213.1:p.Lys558Gln | |
| NM_001093772.1:c.1660A>C | NP_001087241.1:p.Lys554Gln | |
| XM_005265740.1:c.1675A>C | XP_005265797.1:p.Lys559Gln | |
| XM_005265741.1:c.1675A>C | XP_005265798.1:p.Lys559Gln | |
| XM_005265742.1:c.1663A>C | XP_005265799.1:p.Lys555Gln | |
| XM_005265742.3:c.1663A>C | XP_005265799.1:p.Lys555Gln | |
| XM_017008178.1:c.1672A>C | XP_016863667.1:p.Lys558Gln | |
| XM_017008179.1:c.1663A>C | XP_016863668.1:p.Lys555Gln | |
| XM_017008180.1:c.1660A>C | XP_016863669.1:p.Lys554Gln | |
| NM_000222.3:c.1672A>C MANE Select | NP_000213.1:p.Lys558Gln | |
| NM_001093772.2:c.1660A>C | NP_001087241.1:p.Lys554Gln | |
| NM_001385284.1:c.1675A>C | NP_001372213.1:p.Lys559Gln | |
| NM_001385285.1:c.1672A>C | NP_001372214.1:p.Lys558Gln | |
| NM_001385286.1:c.1660A>C | NP_001372215.1:p.Lys554Gln | |
| NM_001385288.1:c.1663A>C | NP_001372217.1:p.Lys555Gln | |
| NM_001385290.1:c.1675A>C | NP_001372219.1:p.Lys559Gln | |
| NM_001385292.1:c.1663A>C | NP_001372221.1:p.Lys555Gln |