Linked Data
ClinVar Variation Id:
215185
dbSNP Id:
rs767820132
ExAC:
16:89590440 G / A
gnomAD v2:
16-89590440-G-A
gnomAD v3:
16-89524032-G-A
gnomAD v4:
16-89524032-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89524032G>A , CM000678.2:g.89524032G>A | GRCh38 |
| NC_000016.9:g.89590440G>A , CM000678.1:g.89590440G>A | GRCh37 |
| NC_000016.8:g.88117941G>A | NCBI36 |
| NG_008082.1:g.20636G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268704.7:c.403G>A | ENSP00000268704.3:p.Asp135Asn | |
| ENST00000562775.2:n.267G>A | ||
| ENST00000564047.2:n.412G>A | ||
| ENST00000564409.2:c.172G>A | ENSP00000495297.1:p.Asp58Asn | |
| ENST00000566371.6:c.403G>A | ENSP00000454475.2:p.Asp135Asn | |
| ENST00000642334.1:c.276G>A | ||
| ENST00000642371.1:c.335G>A | ||
| ENST00000642436.1:n.388+10995G>A | ||
| ENST00000643105.1:c.323G>A | ||
| ENST00000643178.1:n.51G>A | ||
| ENST00000643307.1:c.403G>A | ENSP00000495673.1:p.Asp135Asn | |
| ENST00000643345.1:c.377-5103G>A | ENSP00000493982.1:n.377-5103G>A | |
| ENST00000643496.1:n.220G>A | ||
| ENST00000643649.1:c.403G>A | ENSP00000494806.1:p.Asp135Asn | |
| ENST00000643668.1:c.*431G>A | ENSP00000494903.1:n.*431G>A | |
| ENST00000643724.1:c.403G>A | ENSP00000496335.1:p.Asp135Asn | |
| ENST00000643954.1:c.141G>A | ||
| ENST00000643957.1:c.564G>A | ENSP00000494246.1:n.564G>A | |
| ENST00000644210.1:c.403G>A | ENSP00000495675.1:p.Asp135Asn | |
| ENST00000644225.1:n.420G>A | ||
| ENST00000644498.1:c.403G>A | ENSP00000496244.1:p.Asp135Asn | |
| ENST00000644671.1:c.66G>A | ||
| ENST00000644748.1:n.1834G>A | ||
| ENST00000644781.1:c.403G>A | ENSP00000495473.1:p.Asp135Asn | |
| ENST00000644901.1:c.403G>A | ENSP00000493797.1:p.Asp135Asn | |
| ENST00000645042.1:c.403G>A | ENSP00000493908.1:p.Asp135Asn | |
| ENST00000645063.1:c.403G>A | ENSP00000493590.1:p.Asp135Asn | |
| ENST00000645354.1:c.318G>A | ||
| ENST00000645533.1:c.403G>A | ENSP00000495690.1:p.Asp135Asn | |
| ENST00000645818.2:c.403G>A MANE Select | ENSP00000495795.2:p.Asp135Asn | |
| ENST00000645897.1:c.403G>A | ENSP00000495293.1:p.Asp135Asn | |
| ENST00000645977.1:n.418G>A | ||
| ENST00000646263.1:c.403G>A | ENSP00000494119.1:p.Asp135Asn | |
| ENST00000646303.1:c.271G>A | ENSP00000494160.1:p.Asp91Asn | |
| ENST00000646399.1:c.86G>A | ||
| ENST00000646445.1:c.182+10995G>A | ||
| ENST00000646531.1:c.403G>A | ENSP00000495185.1:p.Asp135Asn | |
| ENST00000646589.1:c.377-6651G>A | ENSP00000494739.1:n.377-6651G>A | |
| ENST00000646716.1:c.376+10995G>A | ENSP00000495593.1:n.376+10995G>A | |
| ENST00000646826.1:c.403G>A | ENSP00000495123.1:p.Asp135Asn | |
| ENST00000646930.1:c.403G>A | ENSP00000495219.1:p.Asp135Asn | |
| ENST00000646958.1:n.353G>A | ||
| ENST00000647032.1:c.18G>A | ||
| ENST00000647079.1:c.-6G>A | ENSP00000495967.1:n.-6G>A | |
| ENST00000647227.1:c.166G>A | ||
| ENST00000268704.6:c.403G>A | ENSP00000268704.2:p.Asp135Asn | |
| ENST00000341316.6:c.403G>A | ENSP00000341157.2:p.Asp135Asn | |
| ENST00000562775.1:n.1313G>A | ||
| ENST00000566371.5:c.271G>A | ENSP00000454475.1:p.Asp91Asn | |
| ENST00000568151.1:c.499G>A | ENSP00000457719.1:p.Asp167Asn | |
| ENST00000620811.4:c.-1174G>A | ENSP00000478030.1:n.-1174G>A | |
| NM_003119.3:c.403G>A | NP_003110.1:p.Asp135Asn | |
| NM_199367.2:c.403G>A | NP_955399.1:p.Asp135Asn | |
| XM_005256321.3:c.403G>A | XP_005256378.1:p.Asp135Asn | |
| XM_006721264.2:c.403G>A | XP_006721327.1:p.Asp135Asn | |
| XM_011523306.1:c.403G>A | XP_011521608.1:p.Asp135Asn | |
| XM_011523307.1:c.403G>A | XP_011521609.1:p.Asp135Asn | |
| NM_001363850.1:c.403G>A | NP_001350779.1:p.Asp135Asn | |
| XM_005256321.4:c.403G>A | XP_005256378.1:p.Asp135Asn | |
| XM_006721264.4:c.403G>A | XP_006721327.1:p.Asp135Asn | |
| XM_017023597.1:c.403G>A | XP_016879086.1:p.Asp135Asn | |
| XM_017023598.1:c.403G>A | XP_016879087.1:p.Asp135Asn | |
| XR_001751971.2:n.442G>A | ||
| XR_001751972.2:n.442G>A | ||
| NM_003119.4:c.403G>A MANE Select | NP_003110.1:p.Asp135Asn | |
| NM_199367.3:c.403G>A | NP_955399.1:p.Asp135Asn |