Linked Data
ClinVar Variation Id:
232111
dbSNP Id:
rs374395284
ExAC:
22:29095872 T / G
gnomAD v2:
22-29095872-T-G
gnomAD v3:
22-28699884-T-G
gnomAD v4:
22-28699884-T-G
PubMed:
PMID:16835864
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.28699884T>G , CM000684.2:g.28699884T>G | GRCh38 |
| NC_000022.10:g.29095872T>G , CM000684.1:g.29095872T>G | GRCh37 |
| NC_000022.9:g.27425872T>G | NCBI36 |
| NG_008150.1:g.46951A>C | |
| NG_008150.2:g.46983A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000439346.6:c.871A>C | ENSP00000396903.2:n.871A>C | |
| ENST00000711048.1:c.962A>C | ENSP00000518557.1:p.Glu321Ala | |
| ENST00000402731.6:c.761A>C | ENSP00000384835.2:p.Glu254Ala | |
| ENST00000404276.6:c.962A>C MANE Select | ENSP00000385747.1:p.Glu321Ala | |
| ENST00000425190.7:c.299A>C | ENSP00000390244.2:p.Glu100Ala | |
| ENST00000464581.6:c.302A>C | ENSP00000483777.2:p.Glu101Ala | |
| ENST00000648295.1:n.514A>C | ||
| ENST00000649563.1:c.299A>C | ENSP00000496928.1:p.Glu100Ala | |
| ENST00000650281.1:c.962A>C | ENSP00000497000.1:p.Glu321Ala | |
| ENST00000328354.10:c.962A>C | ENSP00000329178.6:p.Glu321Ala | |
| ENST00000348295.7:c.962A>C | ENSP00000329012.5:p.Glu321Ala | |
| ENST00000382580.6:c.1091A>C | ENSP00000372023.2:p.Glu364Ala | |
| ENST00000402731.5:c.962A>C | ENSP00000384835.1:p.Glu321Ala | |
| ENST00000403642.5:c.689A>C | ENSP00000384919.1:p.Glu230Ala | |
| ENST00000404276.5:c.962A>C | ENSP00000385747.1:p.Glu321Ala | |
| ENST00000405598.5:c.962A>C | ENSP00000386087.1:p.Glu321Ala | |
| ENST00000416671.5:c.*452A>C | ENSP00000402225.1:n.*452A>C | |
| ENST00000417588.5:c.871A>C | ENSP00000412901.1:n.871A>C | |
| ENST00000425190.6:c.299A>C | ENSP00000390244.1:p.Glu100Ala | |
| ENST00000433028.6:c.*687A>C | ENSP00000403659.1:n.*687A>C | |
| ENST00000433728.5:c.900A>C | ENSP00000404400.1:n.900A>C | |
| ENST00000434810.5:c.193A>C | ||
| ENST00000439346.5:c.433A>C | ENSP00000396903.1:n.433A>C | |
| ENST00000447421.5:c.761A>C | ENSP00000397478.2:p.Glu254Ala | |
| ENST00000448511.5:c.852A>C | ENSP00000404567.1:n.852A>C | |
| ENST00000456369.5:c.217A>C | ||
| ENST00000464581.5:c.302A>C | ENSP00000483777.1:p.Glu101Ala | |
| ENST00000491919.5:n.519A>C | ||
| NM_001005735.1:c.1091A>C | NP_001005735.1:p.Glu364Ala | |
| NM_001257387.1:c.299A>C | NP_001244316.1:p.Glu100Ala | |
| NM_007194.3:c.962A>C | NP_009125.1:p.Glu321Ala | |
| NM_145862.2:c.962A>C | NP_665861.1:p.Glu321Ala | |
| XM_006724114.2:c.482A>C | XP_006724177.1:p.Glu161Ala | |
| XM_006724116.2:c.419A>C | XP_006724179.2:p.Glu140Ala | |
| XM_011529839.1:c.1121A>C | XP_011528141.1:p.Glu374Ala | |
| XM_011529840.1:c.1121A>C | XP_011528142.1:p.Glu374Ala | |
| XM_011529841.1:c.890A>C | XP_011528143.1:p.Glu297Ala | |
| XM_011529842.1:c.791A>C | XP_011528144.1:p.Glu264Ala | |
| XM_011529843.1:c.761A>C | XP_011528145.1:p.Glu254Ala | |
| XM_011529844.1:c.1121A>C | XP_011528146.1:p.Glu374Ala | |
| XM_011529845.1:c.299A>C | XP_011528147.1:p.Glu100Ala | |
| XR_937805.1:n.1121A>C | ||
| XR_937806.1:n.1116A>C | ||
| XR_937807.1:n.1116A>C | ||
| NM_001349956.1:c.761A>C | NP_001336885.1:p.Glu254Ala | |
| NM_007194.4:c.962A>C MANE Select | NP_009125.1:p.Glu321Ala | |
| XM_006724114.3:c.515A>C | XP_006724177.2:p.Glu172Ala | |
| XM_011529839.2:c.1121A>C | XP_011528141.1:p.Glu374Ala | |
| XM_011529840.3:c.1121A>C | XP_011528142.1:p.Glu374Ala | |
| XM_011529842.2:c.791A>C | XP_011528144.1:p.Glu264Ala | |
| XM_011529844.2:c.1121A>C | XP_011528146.1:p.Glu374Ala | |
| XM_011529845.2:c.299A>C | XP_011528147.1:p.Glu100Ala | |
| XM_017028560.1:c.1085A>C | XP_016884049.1:p.Glu362Ala | |
| XM_017028561.2:c.299A>C | XP_016884050.1:p.Glu100Ala | |
| XM_024452148.1:c.992A>C | XP_024307916.1:p.Glu331Ala | |
| XM_024452149.1:c.992A>C | XP_024307917.1:p.Glu331Ala | |
| XR_937805.2:n.1132A>C | ||
| XR_937806.2:n.1132A>C | ||
| XR_937807.2:n.1132A>C | ||
| NM_001005735.2:c.1091A>C | NP_001005735.1:p.Glu364Ala | |
| NM_001257387.2:c.299A>C | NP_001244316.1:p.Glu100Ala | |
| NM_001349956.2:c.761A>C | NP_001336885.1:p.Glu254Ala |