Linked Data
ClinVar Variation Id:
336015
ClinVar RCV Id:
RCV000345549
RCV000379826
RCV000525329
RCV000764404
RCV001261115
RCV001590981
RCV001175064
RCV001813466
RCV002348087
dbSNP Id:
rs371408734
ExAC:
2:39213258 G / C
gnomAD v2:
2-39213258-G-C
gnomAD v3:
2-38986117-G-C
gnomAD v4:
2-38986117-G-C
COSMIC:
COSM3184101
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.38986117G>C , CM000664.2:g.38986117G>C | GRCh38 |
| NC_000002.11:g.39213258G>C , CM000664.1:g.39213258G>C | GRCh37 |
| NC_000002.10:g.39066762G>C | NCBI36 |
| NG_007530.1:g.139347C>G , LRG_754:g.139347C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685279.1:c.2476C>G | ENSP00000509424.1:p.Pro826Ala | |
| ENST00000686849.1:n.500C>G | ||
| ENST00000690876.1:c.*1015C>G | ENSP00000508955.1:n.*1015C>G | |
| ENST00000692089.1:c.3399+1356C>G | ENSP00000508626.1:n.3399+1356C>G | |
| ENST00000692227.1:c.1162-754C>G | ENSP00000509138.1:n.1162-754C>G | |
| ENST00000402219.8:c.3709C>G MANE Select | ENSP00000384675.2:p.Pro1237Ala | |
| ENST00000395038.6:c.3664C>G | ENSP00000378479.2:p.Pro1222Ala | |
| ENST00000402219.6:c.3709C>G | ENSP00000384675.2:p.Pro1237Ala | |
| ENST00000426016.5:c.3709C>G | ENSP00000387784.1:p.Pro1237Ala | |
| ENST00000469581.1:n.452C>G | ||
| NM_005633.3:c.3709C>G , LRG_754t1:c.3709C>G | NP_005624.2:p.Pro1237Ala | |
| XM_005264515.3:c.3664C>G | XP_005264572.1:p.Pro1222Ala | |
| XM_011533060.1:c.3802C>G | XP_011531362.1:p.Pro1268Ala | |
| XM_011533061.1:c.3757C>G | XP_011531363.1:p.Pro1253Ala | |
| XM_011533062.1:c.3688C>G | XP_011531364.1:p.Pro1230Ala | |
| XM_011533063.1:c.3685C>G | XP_011531365.1:p.Pro1229Ala | |
| XM_011533064.1:c.3538C>G | XP_011531366.1:p.Pro1180Ala | |
| XM_011533065.1:c.3604-754C>G | XP_011531367.1:n.3604-754C>G | |
| XM_011533066.1:c.2644C>G | XP_011531368.1:p.Pro882Ala | |
| XM_005264515.4:c.3664C>G | XP_005264572.1:p.Pro1222Ala | |
| XM_011533062.2:c.3688C>G | XP_011531364.1:p.Pro1230Ala | |
| XM_011533064.2:c.3538C>G | XP_011531366.1:p.Pro1180Ala | |
| NM_001382394.1:c.3688C>G | NP_001369323.1:p.Pro1230Ala | |
| NM_001382395.1:c.3664C>G | NP_001369324.1:p.Pro1222Ala | |
| NM_005633.4:c.3709C>G MANE Select | NP_005624.2:p.Pro1237Ala |