Linked Data
ClinVar Variation Id:
2709142
ClinVar RCV Id:
RCV003503683
MyVariant Identifiers:
chr15:g.72641593A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.72349252A>C , CM000677.2:g.72349252A>C | GRCh38 |
| NC_000015.9:g.72641593A>C , CM000677.1:g.72641593A>C | GRCh37 |
| NC_000015.8:g.70428647A>C | NCBI36 |
| NG_009017.1:g.31928T>G | |
| NG_009017.2:g.31928T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000563908.2:n.3159T>G | ||
| ENST00000567027.6:c.813T>G | ENSP00000457521.2:p.Pro271= | |
| ENST00000682061.1:c.*475T>G | ENSP00000508316.1:n.*475T>G | |
| ENST00000682177.1:c.856T>G | ENSP00000507409.1:n.856T>G | |
| ENST00000682461.1:c.919T>G | ENSP00000507308.1:n.919T>G | |
| ENST00000682653.1:n.844T>G | ||
| ENST00000682657.1:c.*223T>G | ENSP00000507753.1:n.*223T>G | |
| ENST00000682721.1:c.*616T>G | ENSP00000507535.1:n.*616T>G | |
| ENST00000682843.1:c.*711T>G | ENSP00000508173.1:n.*711T>G | |
| ENST00000683003.1:c.*223T>G | ENSP00000507576.1:n.*223T>G | |
| ENST00000683133.1:c.997T>G | ENSP00000508108.1:n.997T>G | |
| ENST00000683228.1:n.844T>G | ||
| ENST00000683243.1:c.*223T>G | ENSP00000507042.1:n.*223T>G | |
| ENST00000683463.1:c.813T>G | ENSP00000507986.1:p.Pro271= | |
| ENST00000683548.1:n.844T>G | ||
| ENST00000683579.1:c.*711T>G | ENSP00000506867.1:n.*711T>G | |
| ENST00000683587.1:n.844T>G | ||
| ENST00000683681.1:c.813T>G | ENSP00000508110.1:p.Pro271= | |
| ENST00000683735.1:c.*711T>G | ENSP00000508336.1:n.*711T>G | |
| ENST00000683742.1:n.644T>G | ||
| ENST00000683853.1:c.813T>G | ENSP00000506834.1:p.Pro271= | |
| ENST00000683860.1:c.813T>G | ENSP00000507179.1:p.Pro271= | |
| ENST00000683884.1:c.813T>G | ENSP00000507004.1:p.Pro271= | |
| ENST00000684041.1:c.813T>G | ENSP00000508382.1:p.Pro271= | |
| ENST00000684125.1:c.813T>G | ENSP00000507320.1:p.Pro271= | |
| ENST00000684203.1:n.2651T>G | ||
| ENST00000684231.1:c.*223T>G | ENSP00000507748.1:n.*223T>G | |
| ENST00000684263.1:c.813T>G | ENSP00000508369.1:p.Pro271= | |
| ENST00000684305.1:c.1261T>G | ENSP00000506819.1:n.1261T>G | |
| ENST00000684415.1:c.813T>G | ENSP00000507227.1:p.Pro271= | |
| ENST00000684520.1:c.813T>G | ENSP00000506826.1:p.Pro271= | |
| ENST00000684602.1:c.*479T>G | ENSP00000507996.1:n.*479T>G | |
| ENST00000684667.1:c.1144T>G | ENSP00000507003.1:n.1144T>G | |
| ENST00000268097.10:c.813T>G MANE Select | ENSP00000268097.6:p.Pro271= | |
| ENST00000268097.9:c.813T>G | ENSP00000268097.5:p.Pro271= | |
| ENST00000379915.4:c.413-2927T>G | ENSP00000478716.1:n.413-2927T>G | |
| ENST00000563762.5:c.739-1118T>G | ENSP00000456346.1:n.739-1118T>G | |
| ENST00000566304.5:c.846T>G | ENSP00000455114.1:p.Pro282= | |
| ENST00000566672.5:c.*223T>G | ENSP00000457037.1:n.*223T>G | |
| ENST00000567027.5:c.685T>G | ||
| ENST00000567159.5:c.813T>G | ENSP00000456489.1:p.Pro271= | |
| ENST00000567411.5:c.*334T>G | ENSP00000455545.1:n.*334T>G | |
| ENST00000568777.5:n.6217T>G | ||
| ENST00000569410.5:c.813T>G | ENSP00000457125.1:p.Pro271= | |
| NM_000520.4:c.813T>G | NP_000511.2:p.Pro271= | |
| NM_000520.5:c.813T>G | NP_000511.2:p.Pro271= | |
| NM_001318825.1:c.846T>G | NP_001305754.1:p.Pro282= | |
| NR_134869.1:n.1314T>G | ||
| NM_000520.6:c.813T>G MANE Select | NP_000511.2:p.Pro271= | |
| NM_001318825.2:c.846T>G | NP_001305754.1:p.Pro282= | |
| NR_134869.2:n.855T>G | ||
| NR_134869.3:n.855T>G |