Linked Data
ClinVar Variation Id:
927484
dbSNP Id:
rs2061317060
gnomAD v3:
17-61683859-A-G
gnomAD v4:
17-61683859-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.61683859A>G , CM000679.2:g.61683859A>G | GRCh38 |
| NC_000017.10:g.59761220A>G , CM000679.1:g.59761220A>G | GRCh37 |
| NC_000017.9:g.57116002A>G | NCBI36 |
| NG_007409.2:g.184701T>C , LRG_300:g.184701T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682073.1:n.1927T>C | ||
| ENST00000682453.1:c.3187T>C | ENSP00000506943.1:p.Ser1063Pro | |
| ENST00000682477.1:c.*2613T>C | ENSP00000507075.1:n.*2613T>C | |
| ENST00000682589.1:n.9064T>C | ||
| ENST00000682755.1:c.2965T>C | ENSP00000507660.1:p.Ser989Pro | |
| ENST00000682989.1:c.*278T>C | ENSP00000507786.1:n.*278T>C | |
| ENST00000683039.1:c.3187T>C | ENSP00000508303.1:p.Ser1063Pro | |
| ENST00000683235.1:c.*602T>C | ENSP00000507646.1:n.*602T>C | |
| ENST00000683535.1:n.1317T>C | ||
| ENST00000684584.1:c.2350T>C | ENSP00000508044.1:p.Ser784Pro | |
| ENST00000684626.1:n.1433T>C | ||
| ENST00000684769.1:c.1377T>C | ENSP00000507691.1:n.1377T>C | |
| ENST00000259008.7:c.3187T>C MANE Select | ENSP00000259008.2:p.Ser1063Pro | |
| ENST00000259008.6:c.3187T>C | ENSP00000259008.2:p.Ser1063Pro | |
| NM_032043.2:c.3187T>C , LRG_300t1:c.3187T>C | NP_114432.2:p.Ser1063Pro | |
| XM_011525332.1:c.3247T>C | XP_011523634.1:p.Ser1083Pro | |
| XM_011525333.1:c.3247T>C | XP_011523635.1:p.Ser1083Pro | |
| XM_011525334.1:c.3247T>C | XP_011523636.1:p.Ser1083Pro | |
| XM_011525335.1:c.3187T>C | XP_011523637.1:p.Ser1063Pro | |
| XM_011525336.1:c.3127T>C | XP_011523638.1:p.Ser1043Pro | |
| XM_011525337.1:c.3046T>C | XP_011523639.1:p.Ser1016Pro | |
| XM_011525338.1:c.2764T>C | XP_011523640.1:p.Ser922Pro | |
| XM_011525332.3:c.3247T>C | XP_011523634.1:p.Ser1083Pro | |
| XM_011525333.3:c.3247T>C | XP_011523635.1:p.Ser1083Pro | |
| XM_011525334.2:c.3247T>C | XP_011523636.1:p.Ser1083Pro | |
| XM_011525335.3:c.3187T>C | XP_011523637.1:p.Ser1063Pro | |
| XM_011525336.2:c.3127T>C | XP_011523638.1:p.Ser1043Pro | |
| XM_011525337.2:c.3046T>C | XP_011523639.1:p.Ser1016Pro | |
| XM_011525338.2:c.2764T>C | XP_011523640.1:p.Ser922Pro | |
| XM_017025200.1:c.2704T>C | XP_016880689.1:p.Ser902Pro | |
| XM_017025201.1:c.2704T>C | XP_016880690.1:p.Ser902Pro | |
| XM_017025202.1:c.1333T>C | XP_016880691.1:p.Ser445Pro | |
| XM_017025203.1:c.1333T>C | XP_016880692.1:p.Ser445Pro | |
| NM_032043.3:c.3187T>C MANE Select | NP_114432.2:p.Ser1063Pro |