Linked Data
ClinVar Variation Id:
486570
dbSNP Id:
rs772233665
ExAC:
9:135771731 G / A
gnomAD v2:
9-135771731-G-A
gnomAD v3:
9-132896344-G-A
gnomAD v4:
9-132896344-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.132896344G>A , CM000671.2:g.132896344G>A | GRCh38 |
| NC_000009.11:g.135771731G>A , CM000671.1:g.135771731G>A | GRCh37 |
| NC_000009.10:g.134761552G>A | NCBI36 |
| NG_012386.1:g.53290C>T , LRG_486:g.53290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000475903.7:c.3383C>T | ENSP00000496126.2:p.Ala1128Val | |
| ENST00000490179.4:c.3386C>T | ENSP00000495533.2:p.Ala1129Val | |
| ENST00000642261.2:c.*1242C>T | ENSP00000494743.2:n.*1242C>T | |
| ENST00000643275.2:c.*1326C>T | ENSP00000495598.2:n.*1326C>T | |
| ENST00000643362.2:c.2999C>T | ENSP00000496398.2:p.Ala1000Val | |
| ENST00000643625.2:c.*1128C>T | ENSP00000495546.2:n.*1128C>T | |
| ENST00000643691.2:c.3023C>T | ENSP00000494916.2:p.Ala1008Val | |
| ENST00000644184.2:c.3344C>T | ENSP00000495428.2:p.Ala1115Val | |
| ENST00000645129.2:c.3230C>T | ENSP00000493639.2:p.Ala1077Val | |
| ENST00000646440.2:c.3386C>T | ENSP00000495830.2:p.Ala1129Val | |
| ENST00000298552.9:c.3386C>T MANE Select | ENSP00000298552.3:p.Ala1129Val | |
| ENST00000642617.1:c.3383C>T | ENSP00000493773.1:p.Ala1128Val | |
| ENST00000642627.1:c.3368C>T | ENSP00000496772.1:p.Ala1123Val | |
| ENST00000642811.1:c.*3156C>T | ENSP00000495554.1:n.*3156C>T | |
| ENST00000643072.1:c.3233C>T | ENSP00000496691.1:p.Ala1078Val | |
| ENST00000643583.1:c.3371C>T | ENSP00000494685.1:p.Ala1124Val | |
| ENST00000643625.1:c.1263C>T | ENSP00000495546.1:n.1263C>T | |
| ENST00000643875.1:c.3386C>T | ENSP00000495158.1:p.Ala1129Val | |
| ENST00000644097.1:c.3383C>T | ENSP00000494682.1:p.Ala1128Val | |
| ENST00000644184.1:c.2081C>T | ENSP00000495428.1:p.Ala694Val | |
| ENST00000644255.1:c.*3153C>T | ENSP00000493608.1:n.*3153C>T | |
| ENST00000644319.1:n.3761C>T | ||
| ENST00000644786.1:n.1045C>T | ||
| ENST00000644882.1:n.2294C>T | ||
| ENST00000645901.1:n.4237C>T | ||
| ENST00000646391.1:c.*3156C>T | ENSP00000494104.1:n.*3156C>T | |
| ENST00000646625.1:c.3386C>T | ENSP00000496263.1:p.Ala1129Val | |
| ENST00000647262.1:n.2351C>T | ||
| ENST00000647279.1:c.*2625C>T | ENSP00000494502.1:n.*2625C>T | |
| ENST00000647534.1:n.2450C>T | ||
| ENST00000298552.7:c.3386C>T | ENSP00000298552.3:p.Ala1129Val | |
| ENST00000440111.6:c.3386C>T | ENSP00000394524.2:p.Ala1129Val | |
| ENST00000545250.5:c.3233C>T | ENSP00000444017.1:p.Ala1078Val | |
| NM_000368.4:c.3386C>T , LRG_486t1:c.3386C>T | NP_000359.1:p.Ala1129Val | |
| NM_001162426.1:c.3383C>T | NP_001155898.1:p.Ala1128Val | |
| NM_001162427.1:c.3233C>T | NP_001155899.1:p.Ala1078Val | |
| XM_005272211.1:c.3386C>T | XP_005272268.1:p.Ala1129Val | |
| XM_006717271.1:c.3386C>T | XP_006717334.1:p.Ala1129Val | |
| XM_011518979.1:c.3386C>T | XP_011517281.1:p.Ala1129Val | |
| NM_001362177.1:c.3023C>T | NP_001349106.1:p.Ala1008Val | |
| XM_011518979.2:c.3386C>T | XP_011517281.1:p.Ala1129Val | |
| XM_017015096.1:c.3386C>T | XP_016870585.1:p.Ala1129Val | |
| XM_017015097.1:c.3386C>T | XP_016870586.1:p.Ala1129Val | |
| XM_017015098.1:c.3383C>T | XP_016870587.1:p.Ala1128Val | |
| XM_017015100.1:c.3023C>T | XP_016870589.1:p.Ala1008Val | |
| XM_017015101.1:c.3020C>T | XP_016870590.1:p.Ala1007Val | |
| NM_000368.5:c.3386C>T MANE Select | NP_000359.1:p.Ala1129Val | |
| NM_001162426.2:c.3383C>T | NP_001155898.1:p.Ala1128Val | |
| NM_001162427.2:c.3233C>T | NP_001155899.1:p.Ala1078Val | |
| NM_001362177.2:c.3023C>T | NP_001349106.1:p.Ala1008Val |