Linked Data
ClinVar Variation Id:
29807
ClinVar RCV Id:
RCV000022680
RCV000022681
RCV000055896
RCV000211752
RCV000207516
RCV000515363
RCV000654966
RCV001089761
RCV002288517
dbSNP Id:
rs387906661
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140801551T>G , CM000669.2:g.140801551T>G | GRCh38 |
| NC_000007.13:g.140501351T>G , CM000669.1:g.140501351T>G | GRCh37 |
| NC_000007.12:g.140147820T>G | NCBI36 |
| NG_007873.3:g.128214A>C , LRG_299:g.128214A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.721A>C MANE Select | ENSP00000493543.1:p.Thr241Pro | |
| ENST00000288602.11:c.721A>C | ENSP00000288602.7:p.Thr241Pro | |
| ENST00000496384.7:c.721A>C | ENSP00000419060.2:p.Thr241Pro | |
| ENST00000497784.2:c.*171A>C | ENSP00000420119.2:n.*171A>C | |
| ENST00000642228.1:c.721A>C | ENSP00000493678.1:p.Thr241Pro | |
| ENST00000642272.1:n.753A>C | ||
| ENST00000642875.1:n.215A>C | ||
| ENST00000643356.1:n.322A>C | ||
| ENST00000644120.1:n.1163A>C | ||
| ENST00000644905.1:n.810A>C | ||
| ENST00000644969.2:c.721A>C MANE Plus Clinical | ENSP00000496776.1:p.Thr241Pro | |
| ENST00000646730.1:c.721A>C | ENSP00000494784.1:p.Thr241Pro | |
| ENST00000646891.1:c.721A>C | ENSP00000493543.1:p.Thr241Pro | |
| ENST00000288602.10:c.721A>C | ENSP00000288602.6:p.Thr241Pro | |
| ENST00000497784.1:c.756A>C | ENSP00000420119.1:n.756A>C | |
| NM_004333.4:c.721A>C , LRG_299t1:c.721A>C | NP_004324.2:p.Thr241Pro | |
| XM_005250045.1:c.721A>C | XP_005250102.1:p.Thr241Pro | |
| XM_005250046.1:c.721A>C | XP_005250103.1:p.Thr241Pro | |
| XM_011516529.1:c.721A>C | XP_011514831.1:p.Thr241Pro | |
| XM_011516530.1:c.721A>C | XP_011514832.1:p.Thr241Pro | |
| XR_242190.1:n.729A>C | ||
| XR_927520.1:n.729A>C | ||
| XR_927521.1:n.729A>C | ||
| XR_927522.1:n.729A>C | ||
| XR_927523.1:n.729A>C | ||
| NM_001354609.1:c.721A>C | NP_001341538.1:p.Thr241Pro | |
| NM_004333.5:c.721A>C | NP_004324.2:p.Thr241Pro | |
| NR_148928.1:n.1026A>C | ||
| XM_017012558.1:c.721A>C | XP_016868047.1:p.Thr241Pro | |
| XM_017012559.1:c.721A>C | XP_016868048.1:p.Thr241Pro | |
| XR_001744857.1:n.729A>C | ||
| XR_001744858.1:n.729A>C | ||
| NM_001354609.2:c.721A>C | NP_001341538.1:p.Thr241Pro | |
| NM_001374244.1:c.721A>C | NP_001361173.1:p.Thr241Pro | |
| NM_001374258.1:c.721A>C MANE Plus Clinical | NP_001361187.1:p.Thr241Pro | |
| NM_004333.6:c.721A>C MANE Select | NP_004324.2:p.Thr241Pro | |
| NM_001378467.1:c.730A>C | NP_001365396.1:p.Thr244Pro | |
| NM_001378468.1:c.721A>C | NP_001365397.1:p.Thr241Pro | |
| NM_001378469.1:c.721A>C | NP_001365398.1:p.Thr241Pro | |
| NM_001378470.1:c.619A>C | NP_001365399.1:p.Thr207Pro | |
| NM_001378471.1:c.721A>C | NP_001365400.1:p.Thr241Pro | |
| NM_001378472.1:c.565A>C | NP_001365401.1:p.Thr189Pro | |
| NM_001378473.1:c.565A>C | NP_001365402.1:p.Thr189Pro | |
| NM_001378474.1:c.721A>C | NP_001365403.1:p.Thr241Pro | |
| NM_001378475.1:c.457A>C | NP_001365404.1:p.Thr153Pro |