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:
409738
ClinVar RCV Id:
RCV000464044
dbSNP Id:
rs1060502550
gnomAD v4:
4-54727488-A-G
COSMIC:
COSM235681
CIViC:
CA16611506
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54727488A>G , CM000666.2:g.54727488A>G | GRCh38 |
| NC_000004.11:g.55593654A>G , CM000666.1:g.55593654A>G | GRCh37 |
| NC_000004.10:g.55288411A>G | NCBI36 |
| NG_007456.1:g.74494A>G , LRG_307:g.74494A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412167.7:c.1711A>G | ENSP00000390987.3:p.Thr571Ala | |
| ENST00000685269.1:n.1798A>G | ||
| ENST00000686011.1:c.1708A>G | ENSP00000509704.1:p.Thr570Ala | |
| ENST00000687109.1:c.1723A>G | ENSP00000509371.1:p.Thr575Ala | |
| ENST00000687208.1:n.2135A>G | ||
| ENST00000687246.1:c.1708A>G | ENSP00000509114.1:p.Thr570Ala | |
| ENST00000687265.1:n.1878A>G | ||
| ENST00000687295.1:c.1708A>G | ENSP00000509450.1:p.Thr570Ala | |
| ENST00000689832.1:c.1723A>G | ENSP00000509084.1:p.Thr575Ala | |
| ENST00000689994.1:c.1210A>G | ENSP00000509156.1:p.Thr404Ala | |
| ENST00000690543.1:c.1711A>G | ENSP00000508831.1:p.Thr571Ala | |
| ENST00000690917.1:n.1938A>G | ||
| ENST00000691361.1:n.630A>G | ||
| ENST00000692783.1:c.1720A>G | ENSP00000508733.1:p.Thr574Ala | |
| ENST00000692991.1:n.1817A>G | ||
| ENST00000288135.6:c.1720A>G MANE Select | ENSP00000288135.6:p.Thr574Ala | |
| ENST00000288135.5:c.1720A>G | ENSP00000288135.5:p.Thr574Ala | |
| ENST00000412167.6:c.1708A>G | ENSP00000390987.2:p.Thr570Ala | |
| NM_000222.2:c.1720A>G , LRG_307t1:c.1720A>G | NP_000213.1:p.Thr574Ala | |
| NM_001093772.1:c.1708A>G | NP_001087241.1:p.Thr570Ala | |
| XM_005265740.1:c.1723A>G | XP_005265797.1:p.Thr575Ala | |
| XM_005265741.1:c.1723A>G | XP_005265798.1:p.Thr575Ala | |
| XM_005265742.1:c.1711A>G | XP_005265799.1:p.Thr571Ala | |
| XM_005265742.3:c.1711A>G | XP_005265799.1:p.Thr571Ala | |
| XM_017008178.1:c.1720A>G | XP_016863667.1:p.Thr574Ala | |
| XM_017008179.1:c.1711A>G | XP_016863668.1:p.Thr571Ala | |
| XM_017008180.1:c.1708A>G | XP_016863669.1:p.Thr570Ala | |
| NM_000222.3:c.1720A>G MANE Select | NP_000213.1:p.Thr574Ala | |
| NM_001093772.2:c.1708A>G | NP_001087241.1:p.Thr570Ala | |
| NM_001385284.1:c.1723A>G | NP_001372213.1:p.Thr575Ala | |
| NM_001385285.1:c.1720A>G | NP_001372214.1:p.Thr574Ala | |
| NM_001385286.1:c.1708A>G | NP_001372215.1:p.Thr570Ala | |
| NM_001385288.1:c.1711A>G | NP_001372217.1:p.Thr571Ala | |
| NM_001385290.1:c.1723A>G | NP_001372219.1:p.Thr575Ala | |
| NM_001385292.1:c.1711A>G | NP_001372221.1:p.Thr571Ala |